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Famotidine

NDC 68788-8889, Famotidine, tablet, film coated, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8889
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075718
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8889 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68788-8889-168788888901100 TABLET, FILM COATED in 1 BOTTLE (68788-8889-1)
68788-8889-36878888890330 TABLET, FILM COATED in 1 BOTTLE (68788-8889-3)
68788-8889-66878888890660 TABLET, FILM COATED in 1 BOTTLE (68788-8889-6)
68788-8889-96878888890990 TABLET, FILM COATED in 1 BOTTLE (68788-8889-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5ed77259-5dd9-4634-a073-346693488c4f

Use it

Look up 68788-8889 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8889 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8889. 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.