Product NDC: | 0574-0870 |
Proprietary Name: | ESTRADIOL VALERATE |
Non Proprietary Name: | ESTRADIOL VALERATE |
Active Ingredient(s): | 20 mg/mL & nbsp; ESTRADIOL VALERATE |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0574-0870 |
Labeler Name: | Paddock Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090920 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100331 |
Package NDC: | 0574-0870-05 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0574-0870-05) > 5 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 0574-0870-05 |
Proprietary Name | ESTRADIOL VALERATE |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0574-0870-05) > 5 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 0574-0870 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ESTRADIOL VALERATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 20100331 |
Marketing Category Name | ANDA |
Labeler Name | Paddock Laboratories, Inc. |
Substance Name | ESTRADIOL VALERATE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Estradiol Congeners [Chemical/Ingredient],Estrogen [EPC],Estrogen Receptor Agonists [MoA] |