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Follistim AQ
Follistim AQ - 0052-0308-02 - (follitropin)
Drug Information of Follistim AQ
| Product NDC: | 0052-0308 |
| Proprietary Name: | Follistim AQ |
| Non Proprietary Name: | follitropin |
| Active Ingredient(s): | 75 [iU]/.5mL & nbsp; follitropin |
| Administration Route(s): | INTRAMUSCULAR; SUBCUTANEOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Follistim AQ
| Product NDC: | 0052-0308 |
| Labeler Name: | Organon Pharmaceuticals USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021273 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100628 |
Package Information of Follistim AQ
| Package NDC: | 0052-0308-02 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (0052-0308-02) > .5 mL in 1 VIAL, SINGLE-USE |
NDC Information of Follistim AQ
| NDC Code | 0052-0308-02 |
| Proprietary Name | Follistim AQ |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0052-0308-02) > .5 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0052-0308 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | follitropin |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
| Start Marketing Date | 20100628 |
| Marketing Category Name | NDA |
| Labeler Name | Organon Pharmaceuticals USA |
| Substance Name | FOLLITROPIN |
| Strength Number | 75 |
| Strength Unit | [iU]/.5mL |
| Pharmaceutical Classes | Gonadotropin [EPC],Gonadotropins [Chemical/Ingredient] |
