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Vestura
Vestura - 52544-982-31 - (Drospirenone and Ethinyl Estradiol)
Drug Information of Vestura
| Product NDC: | 52544-982 |
| Proprietary Name: | Vestura |
| Non Proprietary Name: | Drospirenone and Ethinyl Estradiol |
| Active Ingredient(s): | & nbsp; Drospirenone and Ethinyl Estradiol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vestura
| Product NDC: | 52544-982 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078833 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120119 |
Package Information of Vestura
| Package NDC: | 52544-982-31 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (52544-982-31) > 1 KIT in 1 BLISTER PACK (52544-982-28) |
NDC Information of Vestura
| NDC Code | 52544-982-31 |
| Proprietary Name | Vestura |
| Package Description | 3 BLISTER PACK in 1 CARTON (52544-982-31) > 1 KIT in 1 BLISTER PACK (52544-982-28) |
| Product NDC | 52544-982 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Drospirenone and Ethinyl Estradiol |
| Dosage Form Name | KIT |
| Route Name | ORAL |
| Start Marketing Date | 20120119 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
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