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up and up famotidine
up and up famotidine - 11673-061-02 - (Famotidine)
Drug Information of up and up famotidine
| Product NDC: | 11673-061 |
| Proprietary Name: | up and up famotidine |
| 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 up and up famotidine
| Product NDC: | 11673-061 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077351 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120503 |
Package Information of up and up famotidine
| Package NDC: | 11673-061-02 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (11673-061-02) > 5 TABLET in 1 BLISTER PACK |
NDC Information of up and up famotidine
| NDC Code | 11673-061-02 |
| Proprietary Name | up and up famotidine |
| Package Description | 5 BLISTER PACK in 1 CARTON (11673-061-02) > 5 TABLET in 1 BLISTER PACK |
| Product NDC | 11673-061 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Famotidine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120503 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Corporation |
| Substance Name | FAMOTIDINE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
