Orange Book drug · Brand (NDA)

Potassium Chloride 30meq In Dextrose 5% And Sodium Chloride 0.9% In Plastic Container

Dextrose; Potassium Chloride; Sodium Chloride

DiscontinuedRLDNDA 019691 Otsuka Icu Medcl

Approved

Mar 24, 1988

Strengths

Listed patents

Applications

What does the FDA Orange Book show for Potassium Chloride 30meq In Dextrose 5% And Sodium Chloride 0.9% In Plastic Container?

Potassium Chloride 30meq In Dextrose 5% And Sodium Chloride 0.9% In Plastic Container contains Dextrose; Potassium Chloride; Sodium Chloride across 2 FDA applications. NDA 019691 is the lead filing; other filings are listed separately. This page preserves Orange Book facts and source limits. Clinical labeling requires an exact application-matched source.

FDA applications: 2; lead NDA 019691
Lead application holder: Otsuka Icu Medical LLC
Product presentations: 1
Marketing categories: Discontinued
Reference roles: RLD
TE codes: None posted
Listed patents: 0
Exclusivity records: 0

Sourced from the official FDA Orange Book data file · snapshot refreshed Jul 02, 2026, 06:34 PM

FDA product-presentation matrix

Every product number in this exact application

Every FDA product presentation under this application, with strength, dosage form and route, marketing status, therapeutic-equivalence code, and reference role.
Product	Strength	Dosage form / route	Marketing status	TE code	Reference role
007	5GM/100ML;224MG/100ML;900MG/100ML	INJECTABLEINJECTION	Discontinued	None posted	RLD

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

FDA application holder

Otsuka Icu Medical LLC

The Orange Book identifies this organization as the applicant responsible for NDA 019691.

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 on the Discontinued Drug Product List

A discontinued-list entry does not, by itself, show why marketing stopped or whether FDA determined the product was withdrawn for safety or effectiveness.

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

No listed patents or exclusivity records

This means none appear for this application in the current Orange Book files. It is not a freedom-to-operate opinion and does not rule out unlisted patents, regulatory barriers, or product-specific rights.

Same-ingredient landscape

3 other ANDAs and 9 other NDAs found

3 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 019691 appears in 1 comparison cohort. These groups narrow the same-ingredient landscape, but strength and TE code must still match before interpreting therapeutic equivalence.

Injectable · Injection

Dextrose; Potassium Chloride; Sodium Chloride

13 applications

Product rows: 144
Active applications: 11
Active with AB row: 0

Potassium Chloride 0.037% In Dextrose 10% And Sodium Chloride 0.2% In Plastic Container · NDA 019630 Potassium Chloride 10meq In Dextrose 5% And Sodium Chloride 0.3% In Plastic Container · NDA 018876 Potassium Chloride 10meq In Dextrose 5% And Sodium Chloride 0.9% In Plastic Container · NDA 019308 Potassium Chloride 10meq In Dextrose 5% And Sodium Chloride 0.225% In Plastic Container · NDA 018365 Potassium Chloride 10meq In Dextrose 5% And Sodium Chloride 0.45% In Plastic Container · NDA 018362 Dextrose 5%, Sodium Chloride 0.2% And Potassium Chloride 10meq · NDA 018037

Why are clinical sections unavailable?

Exact application-label matching status

Exact source match queuedQueue NDA-019691

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 019691

RLDDiscontinued

Strength: 5GM/100ML;224MG/100ML;900MG/100ML
Dosage form: INJECTABLE
Route: INJECTION
Marketing status: Discontinued

Key dates

Approval, patents, exclusivity

Approval
FDA approval date of this drug product.
Mar 24, 1988
38 yr 11 mo ago
Today

Pharmaceutical detail

FDA product record

Active ingredient

DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE

Strength

5GM/100ML;224MG/100ML;900MG/100ML

Dosage form

INJECTABLE

Route

INJECTION

TE code

Not listed

Application

NDA 019691

Product number

007

Marketing status

Discontinued

Reference listed drug (RLD)

Yes

Reference standard (RS)

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.

Other FDA applications for Potassium Chloride 30meq In Dextrose 5% And Sodium Chloride 0.9% In Plastic Container

1 additional filing

The FDA has approved 2 separate applications under this product name. Each row is one application: a distinct applicant and approval for the same drug.

Other FDA applications approved under the product name Potassium Chloride 30meq In Dextrose 5% And Sodium Chloride 0.9% In Plastic Container, with applicant, approval date, number of strengths, therapeutic-equivalence code, and marketing status.
Application	Applicant	Approved	Strengths	TE code	Status
NDA 019308	Baxter Hlthcare	Apr 05, 1985	1	—	Prescription

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.

View full Dextrose; Potassium Chloride; Sodium Chloride family

How 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

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.