Home
>
National Drug Code (NDC)
>
Famotidine
Famotidine - 61715-064-25 - (famotidine)
Drug Information of Famotidine
| Product NDC: | 61715-064 |
| Proprietary Name: | Famotidine |
| Non Proprietary Name: | famotidine |
| Active Ingredient(s): | 20 mg/1 & nbsp; famotidine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Famotidine
| Product NDC: | 61715-064 |
| Labeler Name: | Kinray |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090283 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120215 |
Package Information of Famotidine
| Package NDC: | 61715-064-25 |
| Package Description: | 1 BOTTLE in 1 CARTON (61715-064-25) > 25 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of Famotidine
| NDC Code | 61715-064-25 |
| Proprietary Name | Famotidine |
| Package Description | 1 BOTTLE in 1 CARTON (61715-064-25) > 25 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 61715-064 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | famotidine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120215 |
| Marketing Category Name | ANDA |
| Labeler Name | Kinray |
| Substance Name | FAMOTIDINE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
