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FAMOTIDINE

NDC 70518-3829, FAMOTIDINE, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-3829
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215630
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3829 \
  -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
70518-3829-17051838290130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-1)
70518-3829-37051838290390 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-3)
70518-3829-47051838290490 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-4)
70518-3829-57051838290530 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-5)
70518-3829-67051838290614 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-6)
70518-3829-77051838290760 TABLET, FILM COATED in 1 BLISTER PACK (70518-3829-7)
70518-3829-87051838290814 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-8)
70518-3829-97051838290925 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3829-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e59a2c97-19c7-485c-bb1b-272ddb9ae053

Use it

Look up 70518-3829 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3829 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3829. 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.