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Leuprolide Acetate
Leuprolide Acetate - 0781-4003-32 - (Leuprolide Acetate)
Drug Information of Leuprolide Acetate
| Product NDC: | 0781-4003 |
| Proprietary Name: | Leuprolide Acetate |
| 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 Leuprolide Acetate
| Product NDC: | 0781-4003 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074728 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980804 |
Package Information of Leuprolide Acetate
| Package NDC: | 0781-4003-32 |
| Package Description: | 1 KIT in 1 CARTON (0781-4003-32) * 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3006-42) > 2.8 mL in 1 VIAL, MULTI-DOSE * 1 mL in 1 PACKET |
NDC Information of Leuprolide Acetate
| NDC Code | 0781-4003-32 |
| Proprietary Name | Leuprolide Acetate |
| Package Description | 1 KIT in 1 CARTON (0781-4003-32) * 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3006-42) > 2.8 mL in 1 VIAL, MULTI-DOSE * 1 mL in 1 PACKET |
| Product NDC | 0781-4003 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Leuprolide Acetate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19980804 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
