Product NDC: | 21695-973 |
Proprietary Name: | Plan B One-Step |
Non Proprietary Name: | levonorgestrel |
Active Ingredient(s): | 1.5 mg/1 & nbsp; levonorgestrel |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-973 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021998 |
Marketing Category: | NDA |
Start Marketing Date: | 20090710 |
Package NDC: | 21695-973-01 |
Package Description: | 1 BLISTER PACK in 1 CARTON (21695-973-01) > 1 TABLET in 1 BLISTER PACK |
NDC Code | 21695-973-01 |
Proprietary Name | Plan B One-Step |
Package Description | 1 BLISTER PACK in 1 CARTON (21695-973-01) > 1 TABLET in 1 BLISTER PACK |
Product NDC | 21695-973 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | levonorgestrel |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090710 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | LEVONORGESTREL |
Strength Number | 1.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Inhibit Ovum Fertilization [PE],Progesterone Congeners [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Progestin-containing Intrauterine Device [EPC] |