| Product NDC: | 68258-3011 | 
| Proprietary Name: | Promethazine Hydrochloride | 
| Non Proprietary Name: | PROMETHAZINE HYDROCHLORIDE | 
| Active Ingredient(s): | 25 mg/1 & nbsp; PROMETHAZINE HYDROCHLORIDE | 
| Administration Route(s): | RECTAL | 
| Dosage Form(s): | SUPPOSITORY | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 68258-3011 | 
| Labeler Name: | Dispensing Solutions Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA123456 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20031219 | 
| Package NDC: | 68258-3011-4 | 
| Package Description: | 1 BLISTER PACK in 1 CARTON (68258-3011-4) > 4 SUPPOSITORY in 1 BLISTER PACK | 
| NDC Code | 68258-3011-4 | 
| Proprietary Name | Promethazine Hydrochloride | 
| Package Description | 1 BLISTER PACK in 1 CARTON (68258-3011-4) > 4 SUPPOSITORY in 1 BLISTER PACK | 
| Product NDC | 68258-3011 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | PROMETHAZINE HYDROCHLORIDE | 
| Dosage Form Name | SUPPOSITORY | 
| Route Name | RECTAL | 
| Start Marketing Date | 20031219 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Dispensing Solutions Inc. | 
| Substance Name | PROMETHAZINE HYDROCHLORIDE | 
| Strength Number | 25 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |