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Famotidine

NDC 68071-2306, Famotidine, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-2306
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075805
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2306 \
  -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
68071-2306-36807123060330 TABLET in 1 BOTTLE (68071-2306-3)
68071-2306-868071230608180 TABLET in 1 BOTTLE (68071-2306-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b556d1a8-4155-50cf-e053-2995a90a9b14

Use it

Look up 68071-2306 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-2306 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-2306. 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.