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TopCare Acid Reducer

NDC 36800-141, Famotidine, tablet, film coated, from Topco Associates LLC.

Product NDC
36800-141
Status
Listed
Labeler
Topco Associates LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA075400
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/36800-141 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
36800-141-653680001416530 BLISTER PACK in 1 CARTON (36800-141-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK
36800-141-72368000141721 BOTTLE in 1 CARTON (36800-141-72) / 60 TABLET, FILM COATED in 1 BOTTLE
36800-141-75368000141751 BOTTLE in 1 CARTON (36800-141-75) / 90 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 36800-141 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/36800-141 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 36800-141. 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.