Search by Drug Name or NDC

NDC 49035-0167-16 Ultra Strength 1000 mg/1 Details

Ultra Strength 1000 mg/1

Ultra Strength is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by Wal-Mart Stores,Inc.,. 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: 49035-0167-16
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	49035-0167
Product ID	49035-167_8ad324cf-763e-4c6e-b383-556b3cba7219
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
Proprietary Name Suffix	Antacid
Non-Proprietary Name	Calcium 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	Wal-Mart Stores,Inc.,
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH DRUG
Application Number	M001
Listing Certified Through	2024-12-31

Package

NDC 49035-0167-16 (49035016716)

Pricing Information	N/A
NDC Package Code	49035-167-16
Billing NDC	49035016716
Package	160 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (49035-167-16)
Marketing Start Date	2019-11-18
NDC Exclude Flag	N