Product NDC: | 56062-194 |
Proprietary Name: | maximum strength |
Non Proprietary Name: | Famotidine |
Active Ingredient(s): | 20 mg/1 & nbsp; Famotidine |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 56062-194 |
Labeler Name: | Publix Super Markets Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA077351 |
Marketing Category: | ANDA |
Start Marketing Date: | 20071203 |
Package NDC: | 56062-194-02 |
Package Description: | 5 BLISTER PACK in 1 CARTON (56062-194-02) > 5 TABLET in 1 BLISTER PACK |
NDC Code | 56062-194-02 |
Proprietary Name | maximum strength |
Package Description | 5 BLISTER PACK in 1 CARTON (56062-194-02) > 5 TABLET in 1 BLISTER PACK |
Product NDC | 56062-194 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Famotidine |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20071203 |
Marketing Category Name | ANDA |
Labeler Name | Publix Super Markets Inc |
Substance Name | FAMOTIDINE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes |