Product ID | 59556-282_7a2ca863-fe8b-4ee6-9a63-40276db84b77 |
NDC | 59556-282 |
Product Type | Human Otc Drug |
Proprietary Name | Levonorgestrel Tablet, 1.5 mg |
Generic Name | Levonorgestrel Tablet, 1.5 Mg |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2022-09-13 |
Marketing Category | ANDA / |
Application Number | ANDA202380 |
Labeler Name | Strides Pharma Inc |
Substance Name | LEVONORGESTREL |
Active Ingredient Strength | 2 mg/1 |
Pharm Classes | Inhibit Ovum Fertilization [PE], Progesterone Congeners [CS], Progesterone Congeners [CS], Progestin [EPC], Progestin-containing Intrauterine Device [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |