| 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 |