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FAMOTIDINE

NDC 51662-1375, FAMOTIDINE, injection, solution, from HF Acquisition Co LLC, DBA HealthFirst.

Product NDC
51662-1375
Status
Listed
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075813
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1375 \
  -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
51662-1375-1516621375012 mL in 1 VIAL, SINGLE-DOSE (51662-1375-1)
51662-1375-2516621375021 VIAL, SINGLE-DOSE in 1 POUCH (51662-1375-2) / 2 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9948991d-9405-c7c8-e053-2995a90a60ca

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=51662-1375

Use it

Look up 51662-1375 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1375 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1375. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.