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Lupron Depot-PED
Lupron Depot-PED - 0074-2108-03 - (leuprolide acetate)
Drug Information of Lupron Depot-PED
| Product NDC: | 0074-2108 |
| Proprietary Name: | Lupron Depot-PED |
| Non Proprietary Name: | leuprolide acetate |
| Active Ingredient(s): | & nbsp; leuprolide acetate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lupron Depot-PED
| Product NDC: | 0074-2108 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020263 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930416 |
Package Information of Lupron Depot-PED
| Package NDC: | 0074-2108-03 |
| Package Description: | 1 KIT in 1 CARTON (0074-2108-03) * 1 mL in 1 SYRINGE * 1 SWAB in 1 PACKET |
NDC Information of Lupron Depot-PED
| NDC Code | 0074-2108-03 |
| Proprietary Name | Lupron Depot-PED |
| Package Description | 1 KIT in 1 CARTON (0074-2108-03) * 1 mL in 1 SYRINGE * 1 SWAB in 1 PACKET |
| Product NDC | 0074-2108 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | leuprolide acetate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19930416 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
