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Maximum Strength Acid Reducer

NDC 49483-720, Famotidine, tablet, from TIME CAP LABORATORIES,INC.

Product NDC
49483-720
Status
Listed
Labeler
TIME CAP LABORATORIES,INC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA217543
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/49483-720 \
  -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
49483-720-0149483072001100 TABLET in 1 BOTTLE (49483-720-01)
49483-720-2049483072020200 TABLET in 1 BOTTLE (49483-720-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 49483072001

    GET /v1/drugs/nadac/49483072001

Use it

Look up 49483-720 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/49483-720 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 49483-720. 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.