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NDC 37808-042, Famotidine, tablet, film coated, from H E B.

Product NDC
37808-042
Status
Listed
Labeler
H E B
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/37808-042 \
  -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
37808-042-63378080042631 BOTTLE in 1 CARTON (37808-042-63) / 25 TABLET, FILM COATED in 1 BOTTLE
37808-042-71378080042711 BOTTLE in 1 CARTON (37808-042-71) / 50 TABLET, FILM COATED in 1 BOTTLE
37808-042-82378080042821 BOTTLE in 1 CARTON (37808-042-82) / 200 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 37808-042 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/37808-042 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 37808-042. 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.