Product NDC: | 68180-897 |
Proprietary Name: | Norethindrone and Ethinyl Estradiol and Ferrous Fumarate |
Non Proprietary Name: | Norethindrone and Ethinyl Estradiol |
Active Ingredient(s): | & nbsp; Norethindrone and Ethinyl Estradiol |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68180-897 |
Labeler Name: | Lupin Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021490 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20111004 |
Package NDC: | 68180-897-13 |
Package Description: | 5 POUCH in 1 CARTON (68180-897-13) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
NDC Code | 68180-897-13 |
Proprietary Name | Norethindrone and Ethinyl Estradiol and Ferrous Fumarate |
Package Description | 5 POUCH in 1 CARTON (68180-897-13) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK |
Product NDC | 68180-897 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Norethindrone and Ethinyl Estradiol |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20111004 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Lupin Pharmaceuticals, Inc. |
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Strength Number | |
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