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Famotidine

NDC 68071-3201, Famotidine, tablet, from NuCare Pharmaceuticals, Inc..

Product NDC
68071-3201
Status
Listed
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078916
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3201 \
  -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
68071-3201-26807132010220 TABLET in 1 BOTTLE (68071-3201-2)
68071-3201-36807132010330 TABLET in 1 BOTTLE (68071-3201-3)
68071-3201-66807132010660 TABLET in 1 BOTTLE (68071-3201-6)
68071-3201-868071320108180 TABLET in 1 BOTTLE (68071-3201-8)
68071-3201-96807132010990 TABLET in 1 BOTTLE (68071-3201-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4b820924-24ad-4a2f-e054-00144ff88e88

Use it

Look up 68071-3201 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3201 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3201. 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.