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RANITIDINE

NDC 71993-314, RANITIDINE, tablet, from Atland Pharmaceuticals, LLC.

Product NDC
71993-314
Status
Listed
Labeler
Atland Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211289
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71993-314 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RANITIDINE HYDROCHLORIDE150 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71993-314-307199303143030 TABLET in 1 BOTTLE (71993-314-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fcf27c99-8bd4-41fb-bff8-38fed9de76d9

Use it

Look up 71993-314 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71993-314 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71993-314. 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.