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Ranitidine Hydrochloride

NDC 55111-129, Ranitidine Hydrochloride, capsule, from Dr. Reddy's Laboratories Limited.

Product NDC
55111-129
Status
Listed
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075742
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-129 \
  -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
55111-129-0555111012905500 CAPSULE in 1 BOTTLE (55111-129-05)
55111-129-605511101296060 CAPSULE in 1 BOTTLE (55111-129-60)

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/7bf94bf7-fa11-70be-9f65-fe26a3db5a63

Use it

Look up 55111-129 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-129 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-129. 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.