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Acid Reducer Maximum Strength

NDC 43598-960, Famotidine, tablet, from Dr.Reddys Laboratories Inc..

Product NDC
43598-960
Status
Listed
Labeler
Dr.Reddys Laboratories Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA077367
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-960 \
  -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
43598-960-32435980960321 BOTTLE in 1 CARTON (43598-960-32) / 170 TABLET in 1 BOTTLE
43598-960-65435980960651 BOTTLE in 1 CARTON (43598-960-65) / 65 TABLET in 1 BOTTLE
43598-960-91435980960911 BOTTLE in 1 CARTON (43598-960-91) / 90 TABLET 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 43598-960 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-960 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-960. 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.