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Leuprolide Acetate
Leuprolide Acetate - 0703-4014-18 - (Leuprolide Acetate)
Drug Information of Leuprolide Acetate
| Product NDC: | 0703-4014 |
| Proprietary Name: | Leuprolide Acetate |
| Non Proprietary Name: | Leuprolide Acetate |
| Active Ingredient(s): | 1 mg/.2mL & nbsp; Leuprolide Acetate |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Leuprolide Acetate
| Product NDC: | 0703-4014 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075471 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20001106 |
Package Information of Leuprolide Acetate
| Package NDC: | 0703-4014-18 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 KIT (0703-4014-18) > 2.8 mL in 1 VIAL, MULTI-DOSE (0703-4014-11) |
NDC Information of Leuprolide Acetate
| NDC Code | 0703-4014-18 |
| Proprietary Name | Leuprolide Acetate |
| Package Description | 1 VIAL, MULTI-DOSE in 1 KIT (0703-4014-18) > 2.8 mL in 1 VIAL, MULTI-DOSE (0703-4014-11) |
| Product NDC | 0703-4014 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Leuprolide Acetate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20001106 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | LEUPROLIDE ACETATE |
| Strength Number | 1 |
| Strength Unit | mg/.2mL |
| Pharmaceutical Classes | Gonadotropin Releasing Hormone Receptor Agonist [EPC],Gonadotropin Releasing Hormone Receptor Agonists [MoA] |
