FDA application holder
Banner Life Sciences LLC
The Orange Book identifies this organization as the applicant responsible for NDA 210296.
Orange Book drug · Brand (NDA)
Bafiertam
Monomethyl Fumarate
RLDNDA 210296 Banner Life Sciences
Approved
Apr 28, 2020
Strengths
1
Listed patents
21
What does the FDA Orange Book show for Bafiertam?
Bafiertam contains Monomethyl Fumarate and is the new drug FDA Orange Book record for NDA 210296. The application has 1 presentation with strength, dosage-form, route, status, RLD/RS, TE, patent, and exclusivity context. Current inventory and clinical labeling are not established without an application-matched source.
- FDA application
- NDA 210296
- Application holder
- Banner Life Sciences LLC
- Product presentations
- 1
- Marketing categories
- Prescription
- Reference roles
- RLD / RS
- TE codes
- None posted
- Listed patents
- 21
- Exclusivity records
- 0
New drug application identity from the Orange Book snapshot.
The listed applicant holds the FDA application; this field does not establish the product manufacturer.
Each FDA product number remains tied to its own strength, dosage form, route, and status.
Orange Book marketing categories do not establish real-time inventory or commercial availability.
RLD and RS designations are presentation-specific, not inferred from the trade name.
Therapeutic-equivalence codes apply only within the matching Orange Book product heading.
A zero means none appear in this snapshot, not that no patent rights exist.
FDA exclusivity and listed patent protection are distinct regulatory concepts.
Sourced from the official FDA Orange Book data file · snapshot refreshed
FDA product-presentation matrix
Every product number in this exact application
| Product | Strength | Dosage form / route | Marketing status | TE code | Reference role |
|---|---|---|---|---|---|
| 001 | 95MG | CAPSULE, DELAYED RELEASEORAL | Prescription | None posted | RLDRS |
Marketing status, TE code, RLD, and RS are presentation-level fields. Never transfer one product number's designation to another presentation.
Who is responsible for this application?
Application holder is not the same as manufacturer
Manufacturer status
Not established by the Orange Book
A product-specific FDA label or NDC source must independently identify a manufacturer, labeler, distributor, packager, repackager, or relabeler. The applicant name is not used as a substitute for that evidence.
Regulatory interpretation
What the record means, and what it does not
FDA marketing status
1 presentation listed as prescription
RX and OTC are Orange Book marketing categories, not real-time inventory signals. Confirm current commercial availability with labeling, the application holder, or an authoritative drug listing.
Therapeutic equivalence
No TE code is posted for this application
No TE code does not mean FDA found the product ineffective or non-equivalent. FDA generally publishes TE evaluations for multisource prescription products; single-source and some other products may have no code.
Patent & exclusivity record
21 listed patent expirations and 0 exclusivity dates remain on or after Jul 26, 2026
The latest future date recorded across those files is Feb 27, 2035. Patent and FDA exclusivity operate independently, can overlap, and do not by themselves predict a generic launch date.
Same-ingredient landscape
0 other ANDAs and 0 other NDAs found
0 of the related ANDA applications are not marked discontinued. Sharing an ingredient does not establish pharmaceutical or therapeutic equivalence; strength, dosage form, route, and TE group still matter.
Which products are meaningfully comparable?
Exact ingredient + dosage form + route cohorts
NDA 210296 appears in 1 comparison cohort. These groups narrow the same-ingredient landscape, but strength and TE code must still match before interpreting therapeutic equivalence.
Capsule, Delayed Release · Oral
Monomethyl Fumarate
- Product rows
- 1
- Active applications
- 1
- Active with AB row
- 0
Why are clinical sections unavailable?
Exact application-label matching status
Exact source match queuedQueue NDA-210296
No exact application-level FDA or DailyMed label match has been reviewed for this application. Approved uses, dosing, warnings, adverse reactions, and clinical evidence remain unavailable rather than being inherited from a related brand, generic, or ingredient record.
Until an exact application match passes human review, this page intentionally omits approved uses, dosing, warnings, adverse reactions, mechanism, and clinical-study summaries. It never inherits those claims from an RLD, brand, generic, or same-ingredient product.
Product detail
NDA 210296
RLDRS
- Strength
- 95MG
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Marketing status
- Prescription
Key dates
Approval, patents, exclusivityApproval
FDA approval date of this drug product.
6 yr 4 mo ago
Today
Patent 10098863 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 10105335 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 10105336 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 10105337 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 10918615 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 10918616 expires
Listed method-of-use patent (U-1384) expiration.
in 8 yr 9 mo
Patent 10918617 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 10945985 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 11590095 expires
Listed method-of-use patent (U-1384) expiration.
in 8 yr 9 mo
Patent 11903918 expires
Listed method-of-use patent (U-1384) expiration.
in 8 yr 9 mo
Patent 9326947 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 9326965 expires
Listed method-of-use patent (U-1384) expiration.
in 8 yr 9 mo
Patent 9511043 expires
Listed method-of-use patent (U-1384) expiration.
in 8 yr 9 mo
Patent 9517209 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 9566259 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 9636318 expires
Listed method-of-use patent (U-1384) expiration.
in 8 yr 9 mo
Patent 9636319 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 9814691 expires
Listed method-of-use patent (U-1384) expiration.
in 8 yr 9 mo
Patent 9814692 expires
Listed method-of-use patent (U-1384) expiration.
in 8 yr 9 mo
Patent 9820960 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent 9820961 expires
Listed drug product patent expiration.
in 8 yr 9 mo
Patent & exclusivity timeline
Protection horizonPatent expiryExclusivity endToday
Pharmaceutical detail
FDA product recordActive ingredient
MONOMETHYL FUMARATE
Strength
95MG
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
TE code
Not listed
Application
NDA 210296
Product number
001
Marketing status
Prescription
Reference listed drug (RLD)
Yes
Reference standard (RS)
Yes
Listed patents
Orange Book patent file| Patent | Expires | In | Type |
|---|---|---|---|
| 10098863 | in 8 yr 9 mo | ProductU-1384 | |
| 10105335 | in 8 yr 9 mo | Product | |
| 10105336 | in 8 yr 9 mo | ProductU-1384 | |
| 10105337 | in 8 yr 9 mo | Product | |
| 10918615 | in 8 yr 9 mo | ProductU-1384 | |
| 10918616 | in 8 yr 9 mo | U-1384 | |
| 10918617 | in 8 yr 9 mo | Product | |
| 10945985 | in 8 yr 9 mo | Product | |
| 11590095 | in 8 yr 9 mo | U-1384 | |
| 11903918 | in 8 yr 9 mo | U-1384 | |
| 9326947 | in 8 yr 9 mo | Product | |
| 9326965 | in 8 yr 9 mo | U-1384 | |
| 9511043 | in 8 yr 9 mo | U-1384 | |
| 9517209 | in 8 yr 9 mo | Product | |
| 9566259 | in 8 yr 9 mo | Product | |
| 9636318 | in 8 yr 9 mo | U-1384 | |
| 9636319 | in 8 yr 9 mo | Product | |
| 9814691 | in 8 yr 9 mo | U-1384 | |
| 9814692 | in 8 yr 9 mo | U-1384 | |
| 9820960 | in 8 yr 9 mo | Product | |
| 9820961 | in 8 yr 9 mo | ProductU-1384 |
Active-ingredient family
Brand + generics
This is a reference-listed drug (RLD), the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
No other applications share this active ingredient.
View full Monomethyl Fumarate familyHow to use this record responsibly
Scope, limitations, and primary sources
What to verify before making a decision
- The applicant is the holder of legal responsibility for the application; the Orange Book does not establish that the applicant manufactured or currently markets every listed product.
- RX, OTC, and discontinued are FDA listing categories, not real-time pharmacy inventory or commercial-availability data.
- Therapeutic equivalence applies only within the matching ingredient, dosage form, route, strength, and TE-code group; same ingredient alone is insufficient.
- Listed patent and exclusivity dates are regulatory intelligence, not legal advice, a freedom-to-operate analysis, or a reliable generic-launch forecast.
- The Orange Book is not prescribing information and does not provide indications, dosing, contraindications, adverse reactions, recalls, or current safety communications.
Official FDA references
- Electronic Orange Book record
- Orange Book preface and TE-code policy
- FDA product, patent, and exclusivity data files
Data shown here is normalized for search and comparison. When a regulatory, substitution, launch, or legal decision turns on a field, verify it against the current FDA record and the relevant source document.
Bafiertam: frequently asked questions
Approval, therapeutic equivalence, patents, and exclusivity for this drug, from the FDA Orange Book.
Built directly from the FDA Orange Book product, patent, and exclusivity files refreshed Jul 02, 2026, 06:34 PM. Every strength of NDA 210296 is shown on this page. Interpret patents, exclusivity, availability, and therapeutic equivalence using the limitations above.
Related FDA reference tools
- FDA Purple BookLicensed biologics, biosimilars, interchangeables, BLA records, and exclusivity dates.
- FDA BiosimilarsFDA-approved biosimilars and interchangeable biosimilars, by reference product.
- 510(k) Predicate DatabaseSearch FDA 510(k) clearances and map predicate-device lineage.
- FDA 483 DatabaseFDA Form 483 observations and inspection records by firm, date, and citation.
