| Product NDC: | 55045-1643 | 
| Proprietary Name: | Promethazine Hydrochloride | 
| Non Proprietary Name: | Promethazine Hydrochloride | 
| Active Ingredient(s): | 6.25 mg/5mL & nbsp; Promethazine Hydrochloride | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | SYRUP | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 55045-1643 | 
| Labeler Name: | Dispensing Solutions, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA040643 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20060426 | 
| Package NDC: | 55045-1643-9 | 
| Package Description: | 118 mL in 1 BOTTLE (55045-1643-9) | 
| NDC Code | 55045-1643-9 | 
| Proprietary Name | Promethazine Hydrochloride | 
| Package Description | 118 mL in 1 BOTTLE (55045-1643-9) | 
| Product NDC | 55045-1643 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Promethazine Hydrochloride | 
| Dosage Form Name | SYRUP | 
| Route Name | ORAL | 
| Start Marketing Date | 20060426 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Dispensing Solutions, Inc. | 
| Substance Name | PROMETHAZINE HYDROCHLORIDE | 
| Strength Number | 6.25 | 
| Strength Unit | mg/5mL | 
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |