Home
>
National Drug Code (NDC)
>
acid controller
acid controller - 59779-194-72 - (Famotidine)
Drug Information of acid controller
| Product NDC: | 59779-194 |
| Proprietary Name: | acid controller |
| 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) |
Labeler Information of acid controller
| Product NDC: | 59779-194 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077351 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060928 |
Package Information of acid controller
| Package NDC: | 59779-194-72 |
| Package Description: | 1 BOTTLE in 1 CARTON (59779-194-72) > 60 TABLET in 1 BOTTLE |
NDC Information of acid controller
| NDC Code | 59779-194-72 |
| Proprietary Name | acid controller |
| Package Description | 1 BOTTLE in 1 CARTON (59779-194-72) > 60 TABLET in 1 BOTTLE |
| Product NDC | 59779-194 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060928 |
| Marketing Category Name | ANDA |
| Labeler Name | CVS Pharmacy |
| Substance Name | FAMOTIDINE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
