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NDC 41163-313, Famotidine, tablet, film coated, from United Natural Foods, Inc. dba UNFI.

Product NDC
41163-313
Status
Listed
Labeler
United Natural Foods, Inc. dba UNFI
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA075400
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/41163-313 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
41163-313-654116303136530 BLISTER PACK in 1 CARTON (41163-313-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK
41163-313-724116303137260 BOTTLE in 1 CARTON (41163-313-72) / 1 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 41163-313 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/41163-313 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 41163-313. 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.