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Ranitidine

NDC 62207-773, Ranitidine, tablet, from Granules India Ltd.

Product NDC
62207-773
Status
Listed
Labeler
Granules India Ltd
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA210243
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62207-773 \
  -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
62207-773-36622070773365 BAG in 1 CARTON (62207-773-36) / 10000 TABLET in 1 BAG (62207-773-32)
62207-773-41622070773411 BOTTLE in 1 CARTON (62207-773-41) / 24 TABLET in 1 BOTTLE
62207-773-47622070773471 BOTTLE in 1 CARTON (62207-773-47) / 500 TABLET in 1 BOTTLE
62207-773-58622070773582 BLISTER PACK in 1 CARTON (62207-773-58) / 10 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 62207-773 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62207-773 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62207-773. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.