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Promethazine hydrochloride and phenylephrine hydrochloride
Promethazine hydrochloride and phenylephrine hydrochloride - 0472-1628-04 - (Promethazine hydrochloride and phenylephrine hydrochloride)
Drug Information of Promethazine hydrochloride and phenylephrine hydrochloride
| Product NDC: | 0472-1628 |
| Proprietary Name: | Promethazine hydrochloride and phenylephrine hydrochloride |
| 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) |
Labeler Information of Promethazine hydrochloride and phenylephrine hydrochloride
| Product NDC: | 0472-1628 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088761 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111219 |
Package Information of Promethazine hydrochloride and phenylephrine hydrochloride
| Package NDC: | 0472-1628-04 |
| Package Description: | 118 mL in 1 BOTTLE (0472-1628-04) |
NDC Information of Promethazine hydrochloride and phenylephrine hydrochloride
| NDC Code | 0472-1628-04 |
| Proprietary Name | Promethazine hydrochloride and phenylephrine hydrochloride |
| Package Description | 118 mL in 1 BOTTLE (0472-1628-04) |
| Product NDC | 0472-1628 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Promethazine hydrochloride and phenylephrine hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20111219 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE |
| Strength Number | 5; 6.25 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
