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WYMZYA FE
WYMZYA FE - 68180-898-13 - (norethindrone and ethinyl estradiol, and ferrous fumarate)
Drug Information of WYMZYA FE
| Product NDC: | 68180-898 |
| Proprietary Name: | WYMZYA FE |
| Non Proprietary Name: | norethindrone and ethinyl estradiol, and ferrous fumarate |
| Active Ingredient(s): | & nbsp; norethindrone and ethinyl estradiol, and ferrous fumarate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of WYMZYA FE
| Product NDC: | 68180-898 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021490 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20121219 |
Package Information of WYMZYA FE
| Package NDC: | 68180-898-13 |
| Package Description: | 72 CARTON in 1 CASE (68180-898-13) > 5 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK |
NDC Information of WYMZYA FE
| NDC Code | 68180-898-13 |
| Proprietary Name | WYMZYA FE |
| Package Description | 72 CARTON in 1 CASE (68180-898-13) > 5 CELLO PACK in 1 CARTON > 1 BLISTER PACK in 1 CELLO PACK > 1 KIT in 1 BLISTER PACK |
| Product NDC | 68180-898 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone and ethinyl estradiol, and ferrous fumarate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20121219 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
