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Gonal-f
Gonal-f - 44087-9070-1 - (follitropin alfa)
Drug Information of Gonal-f
| Product NDC: | 44087-9070 |
| Proprietary Name: | Gonal-f |
| Non Proprietary Name: | follitropin alfa |
| Active Ingredient(s): | & nbsp; follitropin alfa |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gonal-f
| Product NDC: | 44087-9070 |
| Labeler Name: | EMD Serono, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020378 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040325 |
Package Information of Gonal-f
| Package NDC: | 44087-9070-1 |
| Package Description: | 1 KIT in 1 CARTON (44087-9070-1) * 2 mL in 1 VIAL * 2 mL in 1 SYRINGE |
NDC Information of Gonal-f
| NDC Code | 44087-9070-1 |
| Proprietary Name | Gonal-f |
| Package Description | 1 KIT in 1 CARTON (44087-9070-1) * 2 mL in 1 VIAL * 2 mL in 1 SYRINGE |
| Product NDC | 44087-9070 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | follitropin alfa |
| Dosage Form Name | KIT |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20040325 |
| Marketing Category Name | NDA |
| Labeler Name | EMD Serono, Inc. |
| Substance Name | |
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