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Calcium carbonate - 0536-3414-10 - (Calcium carbonate)

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Drug Information of Calcium carbonate

Product NDC: 0536-3414
Proprietary Name: Calcium carbonate
Non Proprietary Name: Calcium carbonate
Active Ingredient(s): 648    mg/1 & nbsp;   Calcium carbonate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Calcium carbonate

Product NDC: 0536-3414
Labeler Name: Rugby Laboratories Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part331
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19990412

Package Information of Calcium carbonate

Package NDC: 0536-3414-10
Package Description: 1000 TABLET in 1 BOTTLE (0536-3414-10)

NDC Information of Calcium carbonate

NDC Code 0536-3414-10
Proprietary Name Calcium carbonate
Package Description 1000 TABLET in 1 BOTTLE (0536-3414-10)
Product NDC 0536-3414
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Calcium carbonate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990412
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rugby Laboratories Inc.
Substance Name CALCIUM CARBONATE
Strength Number 648
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Calcium carbonate


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