complete - 37808-546-63 - (Famotidine, Calcium Carbonate, Magnesium Hydroxide)

Alphabetical Index


Drug Information of complete

Product NDC: 37808-546
Proprietary Name: complete
Non Proprietary Name: Famotidine, Calcium Carbonate, Magnesium Hydroxide
Active Ingredient(s): 800; 10; 165    mg/1; mg/1; mg/1 & nbsp;   Famotidine, Calcium Carbonate, Magnesium Hydroxide
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of complete

Product NDC: 37808-546
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20080914

Package Information of complete

Package NDC: 37808-546-63
Package Description: 25 TABLET, CHEWABLE in 1 BOTTLE (37808-546-63)

NDC Information of complete

NDC Code 37808-546-63
Proprietary Name complete
Package Description 25 TABLET, CHEWABLE in 1 BOTTLE (37808-546-63)
Product NDC 37808-546
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine, Calcium Carbonate, Magnesium Hydroxide
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20080914
Marketing Category Name ANDA
Labeler Name H E B
Substance Name CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
Strength Number 800; 10; 165
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of complete


General Information