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NDC 67751-202, Famotidine, Calcium carbonate, and Magnesium hydroxide, tablet, chewable, from Navajo Manufacturing Company Inc.

Product NDC
67751-202
Status
Listed
Labeler
Navajo Manufacturing Company Inc
Dosage form
TABLET, CHEWABLE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
NDA
Application
NDA020958
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67751-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/1
  • CALCIUM CARBONATE800 mg/1
  • MAGNESIUM HYDROXIDE165 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
67751-202-01677510202011 POUCH in 1 CARTON (67751-202-01) / 1 TABLET, CHEWABLE in 1 POUCH
67751-202-02677510202022 POUCH in 1 CARTON (67751-202-02) / 1 TABLET, CHEWABLE in 1 POUCH

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 67751-202 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67751-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67751-202. 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.