Product NDC: | 63323-025 |
Proprietary Name: | Chorionic Gonadotropin |
Non Proprietary Name: | CHORIOGONADOTROPIN ALFA |
Active Ingredient(s): | & nbsp; CHORIOGONADOTROPIN ALFA |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-025 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017067 |
Marketing Category: | NDA |
Start Marketing Date: | 20110421 |
Package NDC: | 63323-025-10 |
Package Description: | 1 KIT in 1 CARTON (63323-025-10) * 10 mL in 1 VIAL, MULTI-DOSE * 10 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 63323-025-10 |
Proprietary Name | Chorionic Gonadotropin |
Package Description | 1 KIT in 1 CARTON (63323-025-10) * 10 mL in 1 VIAL, MULTI-DOSE * 10 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 63323-025 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CHORIOGONADOTROPIN ALFA |
Dosage Form Name | KIT |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20110421 |
Marketing Category Name | NDA |
Labeler Name | APP Pharmaceuticals, LLC |
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