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FAMOTIDINE

NDC 68788-8485, FAMOTIDINE, tablet, film coated, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8485
Status
Listed
Labeler
Preferred Pharmaceuticals 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/68788-8485 \
  -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
68788-8485-36878884850330 TABLET, FILM COATED in 1 BOTTLE (68788-8485-3)
68788-8485-46878884850414 TABLET, FILM COATED in 1 BOTTLE (68788-8485-4)
68788-8485-66878884850660 TABLET, FILM COATED in 1 BOTTLE (68788-8485-6)
68788-8485-96878884850990 TABLET, FILM COATED in 1 BOTTLE (68788-8485-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b445a613-eaa8-45e8-be1f-5848bfd1dd36

Use it

Look up 68788-8485 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8485 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8485. 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.