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NORETHINDRONE
NORETHINDRONE - 68180-876-13 - (NORETHINDRONE)
Drug Information of NORETHINDRONE
| Product NDC: | 68180-876 |
| Proprietary Name: | NORETHINDRONE |
| Non Proprietary Name: | NORETHINDRONE |
| Active Ingredient(s): | .35 mg/1 & nbsp; NORETHINDRONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NORETHINDRONE
| Product NDC: | 68180-876 |
| Labeler Name: | LUPIN PHARMACEUTICALS INC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091325 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111110 |
Package Information of NORETHINDRONE
| Package NDC: | 68180-876-13 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68180-876-13) > 28 TABLET in 1 BLISTER PACK (68180-876-11) |
NDC Information of NORETHINDRONE
| NDC Code | 68180-876-13 |
| Proprietary Name | NORETHINDRONE |
| Package Description | 3 BLISTER PACK in 1 CARTON (68180-876-13) > 28 TABLET in 1 BLISTER PACK (68180-876-11) |
| Product NDC | 68180-876 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NORETHINDRONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111110 |
| Marketing Category Name | ANDA |
| Labeler Name | LUPIN PHARMACEUTICALS INC |
| Substance Name | NORETHINDRONE |
| Strength Number | .35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
