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NDC 63868-0048-72 Quality Choice Ultra Strength 1000 mg/1 Details

Quality Choice Ultra Strength 1000 mg/1

Quality Choice Ultra Strength is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by CHAIN DRUG MARKETING ASSOCIATION. 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: 63868-0048-72
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	63868-0048
Product ID	63868-048_50be20f9-7d12-4c60-acad-d5ba318102f1
Associated GPIs	48300010000545
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	Quality Choice Ultra Strength
Proprietary Name Suffix	Assorted Fruit
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	CHAIN DRUG MARKETING ASSOCIATION
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH DRUG
Application Number	M001
Listing Certified Through	2024-12-31

Package

NDC 63868-0048-72 (63868004872)

Pricing Information	N/A
NDC Package Code	63868-048-72
Billing NDC	63868004872
Package	72 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (63868-048-72)
Marketing Start Date	2019-04-18
NDC Exclude Flag	N