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NDC 0363-0701, Famotidine, tablet, film coated, from Walgreen Company.

Product NDC
0363-0701
Status
Listed
Labeler
Walgreen Company
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA077351
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0363-0701 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0363-0701-82003630701821 BOTTLE in 1 CARTON (0363-0701-82) / 200 TABLET, FILM COATED in 1 BOTTLE
0363-0701-98003630701981 BOTTLE in 1 CARTON (0363-0701-98) / 75 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

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

Use it

Look up 0363-0701 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0363-0701 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0363-0701. 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.