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NDC 0113-6023, famotidine, calcium carbonate and magnesium hydroxide, tablet, chewable, from L. Perrigo Company.

Product NDC
0113-6023
Status
Listed
Labeler
L. Perrigo Company
Dosage form
TABLET, CHEWABLE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA077355
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0113-6023 \
  -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

Calculi Dissolution Agent [EPC]; Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Package NDCNDC-11Package
0113-6023-63001136023631 BOTTLE in 1 CARTON (0113-6023-63) / 25 TABLET, CHEWABLE 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 0113-6023 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0113-6023 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0113-6023. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.