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DROSPIRENONE AND ETHINYL ESTRADIOL
DROSPIRENONE AND ETHINYL ESTRADIOL - 68180-902-13 - (DROSPIRENONE AND ETHINYL ESTRADIOL)
Drug Information of DROSPIRENONE AND ETHINYL ESTRADIOL
| Product NDC: | 68180-902 |
| Proprietary Name: | DROSPIRENONE AND ETHINYL ESTRADIOL |
| 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 DROSPIRENONE AND ETHINYL ESTRADIOL
| Product NDC: | 68180-902 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201663 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121231 |
Package Information of DROSPIRENONE AND ETHINYL ESTRADIOL
| Package NDC: | 68180-902-13 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68180-902-13) > 1 KIT in 1 BLISTER PACK (68180-902-11) |
NDC Information of DROSPIRENONE AND ETHINYL ESTRADIOL
| NDC Code | 68180-902-13 |
| Proprietary Name | DROSPIRENONE AND ETHINYL ESTRADIOL |
| Package Description | 3 BLISTER PACK in 1 CARTON (68180-902-13) > 1 KIT in 1 BLISTER PACK (68180-902-11) |
| Product NDC | 68180-902 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DROSPIRENONE AND ETHINYL ESTRADIOL |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20121231 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
