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Famotidine

NDC 0641-6021, Famotidine, injection, from Hikma Pharmaceuticals USA Inc..

Product NDC
0641-6021
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075488
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6021 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/mL

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]

Package NDCNDC-11Package
0641-6021-100064160211010 VIAL in 1 CARTON (0641-6021-10) / 20 mL in 1 VIAL (0641-6021-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1fdf16e5-145d-4c19-a318-fc6c10794b50
  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0641-6021

Use it

Look up 0641-6021 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6021 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0641-6021. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.