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LEUPROLIDE ACETATE
LEUPROLIDE ACETATE - 41616-936-40 - (LEUPROLIDE ACETATE)
Drug Information of LEUPROLIDE ACETATE
| Product NDC: | 41616-936 |
| Proprietary Name: | LEUPROLIDE ACETATE |
| Non Proprietary Name: | LEUPROLIDE ACETATE |
| Active Ingredient(s): | & nbsp; LEUPROLIDE ACETATE |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEUPROLIDE ACETATE
| Product NDC: | 41616-936 |
| Labeler Name: | Sun Pharma Global Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078885 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090303 |
Package Information of LEUPROLIDE ACETATE
| Package NDC: | 41616-936-40 |
| Package Description: | 1 KIT in 1 CARTON (41616-936-40) * 1 VIAL, MULTI-DOSE in 1 CARTON > 2.8 mL in 1 VIAL, MULTI-DOSE * 1 SWAB in 1 PACKET |
NDC Information of LEUPROLIDE ACETATE
| NDC Code | 41616-936-40 |
| Proprietary Name | LEUPROLIDE ACETATE |
| Package Description | 1 KIT in 1 CARTON (41616-936-40) * 1 VIAL, MULTI-DOSE in 1 CARTON > 2.8 mL in 1 VIAL, MULTI-DOSE * 1 SWAB in 1 PACKET |
| Product NDC | 41616-936 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEUPROLIDE ACETATE |
| Dosage Form Name | KIT |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20090303 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharma Global Inc. |
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