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Famotidine

NDC 70954-316, Famotidine, powder, for suspension, from ANI Pharmaceuticals, Inc..

Product NDC
70954-316
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215043
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-316 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
70954-316-107095403161050 mL in 1 BOTTLE (70954-316-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8e41e259-b161-4f11-a6f7-14e6b60885b8

  • NADAC price for package 70954031610

    GET /v1/drugs/nadac/70954031610

Use it

Look up 70954-316 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-316 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-316. 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.