Product NDC: | 65162-678 |
Proprietary Name: | Promethazine Hydrochloride |
Non Proprietary Name: | Promethazine |
Active Ingredient(s): | 6.25 mg/5mL & nbsp; Promethazine |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65162-678 |
Labeler Name: | Amneal Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040882 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091230 |
Package NDC: | 65162-678-90 |
Package Description: | 473 mL in 1 BOTTLE (65162-678-90) |
NDC Code | 65162-678-90 |
Proprietary Name | Promethazine Hydrochloride |
Package Description | 473 mL in 1 BOTTLE (65162-678-90) |
Product NDC | 65162-678 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Promethazine |
Dosage Form Name | SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20091230 |
Marketing Category Name | ANDA |
Labeler Name | Amneal Pharmaceuticals |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Strength Number | 6.25 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |