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Ranitidine

NDC 0121-0727, RANITIDINE, syrup, from Pharmaceutical Associates, Inc..

Product NDC
0121-0727
Status
Listed
Labeler
Pharmaceutical Associates, Inc.
Dosage form
SYRUP
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077405
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0727 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RANITIDINE15 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
0121-0727-1600121072716473 mL in 1 BOTTLE (0121-0727-16)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d0da9dd6-c691-4614-99c7-531b0bf34837

Use it

Look up 0121-0727 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0727 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-0727. 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.