Product NDC: | 0121-4721 |
Proprietary Name: | Fluoxetine |
Non Proprietary Name: | FLUOXETINE HYDROCHLORIDE |
Active Ingredient(s): | 20 mg/5mL & nbsp; FLUOXETINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0121-4721 |
Labeler Name: | Pharmaceutical Associates, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076015 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020201 |
Package NDC: | 0121-4721-05 |
Package Description: | 5 mL in 1 CUP, UNIT-DOSE (0121-4721-05) |
NDC Code | 0121-4721-05 |
Proprietary Name | Fluoxetine |
Package Description | 5 mL in 1 CUP, UNIT-DOSE (0121-4721-05) |
Product NDC | 0121-4721 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FLUOXETINE HYDROCHLORIDE |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20020201 |
Marketing Category Name | ANDA |
Labeler Name | Pharmaceutical Associates, Inc. |
Substance Name | FLUOXETINE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |