Home
>
National Drug Code (NDC)
>
Lupaneta Pack
Lupaneta Pack - 0074-1052-05 - (leuprolide acetate and norethindrone acetate)
Drug Information of Lupaneta Pack
| Product NDC: | 0074-1052 |
| Proprietary Name: | Lupaneta Pack |
| Non Proprietary Name: | leuprolide acetate and norethindrone acetate |
| Active Ingredient(s): | & nbsp; leuprolide acetate and norethindrone acetate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lupaneta Pack
| Product NDC: | 0074-1052 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA203696 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130701 |
Package Information of Lupaneta Pack
| Package NDC: | 0074-1052-05 |
| Package Description: | 1 KIT in 1 CARTON (0074-1052-05) * 30 TABLET in 1 BOTTLE (0074-1049-02) * 1 mL in 1 PACKET * 1 mL in 1 SYRINGE (0074-3641-04) |
NDC Information of Lupaneta Pack
| NDC Code | 0074-1052-05 |
| Proprietary Name | Lupaneta Pack |
| Package Description | 1 KIT in 1 CARTON (0074-1052-05) * 30 TABLET in 1 BOTTLE (0074-1049-02) * 1 mL in 1 PACKET * 1 mL in 1 SYRINGE (0074-3641-04) |
| Product NDC | 0074-1052 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | leuprolide acetate and norethindrone acetate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20130701 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
