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Lupron Depot
Lupron Depot - 0074-3642-03 - (Leuprorelin Acetate)
Drug Information of Lupron Depot
| Product NDC: | 0074-3642 |
| Proprietary Name: | Lupron Depot |
| Non Proprietary Name: | Leuprorelin Acetate |
| Active Ingredient(s): | & nbsp; Leuprorelin Acetate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lupron Depot
| Product NDC: | 0074-3642 |
| Labeler Name: | Abbott Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019732 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19890126 |
Package Information of Lupron Depot
| Package NDC: | 0074-3642-03 |
| Package Description: | 1 KIT in 1 CARTON * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET |
NDC Information of Lupron Depot
| NDC Code | 0074-3642-03 |
| Proprietary Name | Lupron Depot |
| Package Description | 1 KIT in 1 CARTON * 1 mL in 1 SYRINGE * 1 mL in 1 PACKET |
| Product NDC | 0074-3642 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Leuprorelin Acetate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19890126 |
| Marketing Category Name | NDA |
| Labeler Name | Abbott Laboratories |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
