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Famotidine

NDC 70756-052, Famotidine, tablet, from Lifestar Pharma LLC.

Product NDC
70756-052
Status
Listed
Labeler
Lifestar Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075302
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70756-052 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70756-052-1170756005211100 TABLET in 1 BOTTLE (70756-052-11)
70756-052-12707560052121000 TABLET in 1 BOTTLE (70756-052-12)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/044a510f-33df-4484-8f07-d821f52b9376

  • NADAC price for package 70756005211

    GET /v1/drugs/nadac/70756005211

  • NADAC price for package 70756005212

    GET /v1/drugs/nadac/70756005212

Use it

Look up 70756-052 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70756-052 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70756-052. 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.