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Jolivette
Jolivette - 52544-892-28 - (NORETHINDRONE)
Drug Information of Jolivette
| Product NDC: | 52544-892 |
| Proprietary Name: | Jolivette |
| 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 Jolivette
| Product NDC: | 52544-892 |
| Labeler Name: | Watson Pharma Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016954 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030301 |
Package Information of Jolivette
| Package NDC: | 52544-892-28 |
| Package Description: | 6 BLISTER PACK in 1 BOX (52544-892-28) > 28 TABLET in 1 BLISTER PACK |
NDC Information of Jolivette
| NDC Code | 52544-892-28 |
| Proprietary Name | Jolivette |
| Package Description | 6 BLISTER PACK in 1 BOX (52544-892-28) > 28 TABLET in 1 BLISTER PACK |
| Product NDC | 52544-892 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NORETHINDRONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030301 |
| Marketing Category Name | NDA |
| Labeler Name | Watson Pharma Inc |
| Substance Name | NORETHINDRONE |
| Strength Number | .35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
