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ACID REDUCER

NDC 42507-194, Famotidine, tablet, film coated, from HyVee Inc.

Product NDC
42507-194
Status
Listed
Labeler
HyVee Inc
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/42507-194 \
  -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
42507-194-014250701940125 BLISTER PACK in 1 CARTON (42507-194-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK
42507-194-71425070194711 BOTTLE in 1 CARTON (42507-194-71) / 50 TABLET, FILM COATED in 1 BOTTLE (42507-194-50)
42507-194-78425070194781 BOTTLE in 1 CARTON (42507-194-78) / 100 TABLET, FILM COATED in 1 BOTTLE (42507-194-00)

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 42507-194 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42507-194 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42507-194. 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.