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Gianvi
Gianvi - 0093-5423-58 - (Drospirenone and ethinyl estradiol)
Drug Information of Gianvi
| Product NDC: | 0093-5423 |
| Proprietary Name: | Gianvi |
| Non Proprietary Name: | Drospirenone and ethinyl estradiol |
| Active Ingredient(s): | & nbsp; Drospirenone and ethinyl estradiol |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gianvi
| Product NDC: | 0093-5423 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021676 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20110330 |
Package Information of Gianvi
| Package NDC: | 0093-5423-58 |
| Package Description: | 3 BLISTER PACK in 1 PACKAGE (0093-5423-58) > 1 KIT in 1 BLISTER PACK (0093-5423-28) |
NDC Information of Gianvi
| NDC Code | 0093-5423-58 |
| Proprietary Name | Gianvi |
| Package Description | 3 BLISTER PACK in 1 PACKAGE (0093-5423-58) > 1 KIT in 1 BLISTER PACK (0093-5423-28) |
| Product NDC | 0093-5423 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Drospirenone and ethinyl estradiol |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110330 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
