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RANITIDINE

NDC 64980-637, RANITIDINE, tablet, from Rising Pharma Holdings, Inc..

Product NDC
64980-637
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
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/64980-637 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RANITIDINE HYDROCHLORIDE300 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
64980-637-036498006370330 TABLET in 1 BOTTLE (64980-637-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0fba6615-37c2-4ba6-b6e5-09599369a5bc

Use it

Look up 64980-637 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64980-637 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64980-637. 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.