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Promethazine Hydrochloride and Phenylephrine Hydrochloride
Promethazine Hydrochloride and Phenylephrine Hydrochloride - 65162-679-86 - (Promethazine and Phenylephrine)
Drug Information of Promethazine Hydrochloride and Phenylephrine Hydrochloride
| Product NDC: | 65162-679 |
| Proprietary Name: | Promethazine Hydrochloride and Phenylephrine Hydrochloride |
| Non Proprietary Name: | Promethazine and Phenylephrine |
| Active Ingredient(s): | 5; 6.25 mg/5mL; mg/5mL & nbsp; Promethazine and Phenylephrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Promethazine Hydrochloride and Phenylephrine Hydrochloride
| Product NDC: | 65162-679 |
| Labeler Name: | Amneal Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040902 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090825 |
Package Information of Promethazine Hydrochloride and Phenylephrine Hydrochloride
| Package NDC: | 65162-679-86 |
| Package Description: | 118 mL in 1 BOTTLE (65162-679-86) |
NDC Information of Promethazine Hydrochloride and Phenylephrine Hydrochloride
| NDC Code | 65162-679-86 |
| Proprietary Name | Promethazine Hydrochloride and Phenylephrine Hydrochloride |
| Package Description | 118 mL in 1 BOTTLE (65162-679-86) |
| Product NDC | 65162-679 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Promethazine and Phenylephrine |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090825 |
| Marketing Category Name | ANDA |
| Labeler Name | Amneal Pharmaceuticals |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 5; 6.25 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
