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ELIGARD
ELIGARD - 0024-0222-05 - (leuprolide acetate)
Drug Information of ELIGARD
| Product NDC: | 0024-0222 |
| Proprietary Name: | ELIGARD |
| 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 ELIGARD
| Product NDC: | 0024-0222 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021379 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020123 |
Package Information of ELIGARD
| Package NDC: | 0024-0222-05 |
| Package Description: | 1 KIT in 1 CARTON (0024-0222-05) * .375 mL in 1 SYRINGE * .375 mL in 1 SYRINGE |
NDC Information of ELIGARD
| NDC Code | 0024-0222-05 |
| Proprietary Name | ELIGARD |
| Package Description | 1 KIT in 1 CARTON (0024-0222-05) * .375 mL in 1 SYRINGE * .375 mL in 1 SYRINGE |
| Product NDC | 0024-0222 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | leuprolide acetate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20020123 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
