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NDC 11673-0813-47 ultra strength antacid 1000 mg/1 Details

ultra strength antacid 1000 mg/1

ultra strength antacid is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is CALCIUM CARBONATE.

MedlinePlus Drug Summary

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 11673-0813-47
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	11673-0813
Product ID	11673-813_ac07a7ea-3696-4e06-92fa-243e767eedc4
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	ultra strength antacid
Proprietary Name Suffix	Peppermint Flavored
Non-Proprietary Name	Calciium carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	1000
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	Target Corporation
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH DRUG
Application Number	M001
Listing Certified Through	2024-12-31

Package

NDC 11673-0813-47 (11673081347)

Pricing Information	N/A
NDC Package Code	11673-813-47
Billing NDC	11673081347
Package	160 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (11673-813-47)
Marketing Start Date	2018-03-15
NDC Exclude Flag	N