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FAMOTIDINE

NDC 68071-3413, FAMOTIDINE, tablet, film coated, from NuCare Pharmceuticals,Inc..

Product NDC
68071-3413
Status
Listed
Labeler
NuCare Pharmceuticals,Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215630
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3413 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68071-3413-36807134130330 TABLET, FILM COATED in 1 BOTTLE (68071-3413-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fc603d56-6828-8c5e-e053-6394a90a35bd

Use it

Look up 68071-3413 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3413 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3413. 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.