FDA Orange Book · active-ingredient family
Chromic chloride
Chromic chloride: 2 brands, 1 generic; first approved Jun 26, 1986; generic available.
Generic availableHas discontinued products
Generic status & protection
Generic available: 1 ANDA application approved.
Brands (NDA)
2
Generics (ANDA)
1
Listed patents
0
Presentations
3
Brand (NDA) products
Originator applications
- HOSPIRANDA 0189611986
Approved strengths under this FDA application. Strength Dosage form Route Status TE EQ 0.004MG CHROMIUM/ML INJECTABLE INJECTION Rx AP - CHROMIC CHLORIDEABRAXIS PHARMNDA 0192711987
Approved strengths under this FDA application. Strength Dosage form Route Status TE EQ 0.004MG CHROMIUM/ML INJECTABLE INJECTION Discontinued —
Generic (ANDA) products (1)
Abbreviated applications
- CHROMIC CHLORIDESOMERSET THERAPS LLCANDA 2185382024
Approved strengths under this FDA application. Strength Dosage form Route Status TE EQ 0.004MG CHROMIUM/ML INJECTABLE INJECTION Rx AP
Listed patents
Orange Book patent file
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
Approval history
FDA approval span
First approval
40 yr 9 mo ago
Most recent approval
1 yr 9 mo ago
Approvals span 1986–2024 across 3 FDA applications.
Brand (NDA) 267%
Generic (ANDA) 133%
Chromic chloride: frequently asked questions
Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.
Built directly from the FDA Orange Book data file (products, patents, and exclusivity). TE codes, RLD/RS flags, patent expirations, and exclusivity dates match the official FDA record. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
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.
