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Norethindrone
Norethindrone - 0378-7272-56 - (Norethindrone)
Drug Information of Norethindrone
| Product NDC: | 0378-7272 |
| 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: | 0378-7272 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200980 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130624 |
Package Information of Norethindrone
| Package NDC: | 0378-7272-56 |
| Package Description: | 6 POUCH in 1 CARTON (0378-7272-56) > 1 BLISTER PACK in 1 POUCH > 28 TABLET in 1 BLISTER PACK |
NDC Information of Norethindrone
| NDC Code | 0378-7272-56 |
| Proprietary Name | Norethindrone |
| Package Description | 6 POUCH in 1 CARTON (0378-7272-56) > 1 BLISTER PACK in 1 POUCH > 28 TABLET in 1 BLISTER PACK |
| Product NDC | 0378-7272 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Norethindrone |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130624 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | NORETHINDRONE |
| Strength Number | .35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
