Product NDC: | 54868-3935 |
Proprietary Name: | Promethazine VC |
Non Proprietary Name: | Promethazine Hydrochloride and Phenylephrine Hydrochloride |
Active Ingredient(s): | 5; 6.25 mg/5mL; mg/5mL & nbsp; Promethazine Hydrochloride and Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-3935 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040654 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000906 |
Package NDC: | 54868-3935-0 |
Package Description: | 118 mL in 1 BOTTLE (54868-3935-0) |
NDC Code | 54868-3935-0 |
Proprietary Name | Promethazine VC |
Package Description | 118 mL in 1 BOTTLE (54868-3935-0) |
Product NDC | 54868-3935 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Promethazine Hydrochloride and Phenylephrine Hydrochloride |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20000906 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE |
Strength Number | 5; 6.25 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |