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Pregnyl
Pregnyl - 0052-0315-10 - (CHORIOGONADOTROPIN ALFA)
Drug Information of Pregnyl
| Product NDC: | 0052-0315 |
| Proprietary Name: | Pregnyl |
| Non Proprietary Name: | CHORIOGONADOTROPIN ALFA |
| Active Ingredient(s): | & nbsp; CHORIOGONADOTROPIN ALFA |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pregnyl
| Product NDC: | 0052-0315 |
| Labeler Name: | Organon USA Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017692 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19761020 |
Package Information of Pregnyl
| Package NDC: | 0052-0315-10 |
| Package Description: | 1 KIT in 1 CARTON (0052-0315-10) * 10 mL in 1 VIAL, MULTI-DOSE * 10 mL in 1 VIAL |
NDC Information of Pregnyl
| NDC Code | 0052-0315-10 |
| Proprietary Name | Pregnyl |
| Package Description | 1 KIT in 1 CARTON (0052-0315-10) * 10 mL in 1 VIAL, MULTI-DOSE * 10 mL in 1 VIAL |
| Product NDC | 0052-0315 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHORIOGONADOTROPIN ALFA |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19761020 |
| Marketing Category Name | NDA |
| Labeler Name | Organon USA Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
