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SUPPRELIN
SUPPRELIN - 67979-002-01 - (histrelin acetate)
Drug Information of SUPPRELIN
| Product NDC: | 67979-002 |
| Proprietary Name: | SUPPRELIN |
| Non Proprietary Name: | histrelin acetate |
| Active Ingredient(s): | 50 mg/1 & nbsp; histrelin acetate |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | IMPLANT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUPPRELIN
| Product NDC: | 67979-002 |
| Labeler Name: | Endo Pharmaceuticals Solutions Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022058 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070531 |
Package Information of SUPPRELIN
| Package NDC: | 67979-002-01 |
| Package Description: | 1 VIAL, GLASS in 1 CARTON (67979-002-01) > 1 IMPLANT in 1 VIAL, GLASS |
NDC Information of SUPPRELIN
| NDC Code | 67979-002-01 |
| Proprietary Name | SUPPRELIN |
| Package Description | 1 VIAL, GLASS in 1 CARTON (67979-002-01) > 1 IMPLANT in 1 VIAL, GLASS |
| Product NDC | 67979-002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | histrelin acetate |
| Dosage Form Name | IMPLANT |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20070531 |
| Marketing Category Name | NDA |
| Labeler Name | Endo Pharmaceuticals Solutions Inc. |
| Substance Name | HISTRELIN ACETATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Gonadotropin Releasing Hormone Receptor Agonist [EPC],Gonadotropin Releasing Hormone Receptor Agonists [MoA] |
