Product NDC: | 68016-010 |
Proprietary Name: | Premier Value Famotidine |
Non Proprietary Name: | Famotidine |
Active Ingredient(s): | 10 mg/1 & nbsp; Famotidine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68016-010 |
Labeler Name: | Premier Value |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA090283 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100625 |
Package NDC: | 68016-010-82 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (68016-010-82) |
NDC Code | 68016-010-82 |
Proprietary Name | Premier Value Famotidine |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (68016-010-82) |
Product NDC | 68016-010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Famotidine |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100625 |
Marketing Category Name | ANDA |
Labeler Name | Premier Value |
Substance Name | FAMOTIDINE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes |