| Product NDC: | 0574-7226 | 
| Proprietary Name: | Compro | 
| Non Proprietary Name: | PROCHLORPERAZINE | 
| Active Ingredient(s): | 25 mg/1 & nbsp; PROCHLORPERAZINE | 
| Administration Route(s): | RECTAL | 
| Dosage Form(s): | SUPPOSITORY | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0574-7226 | 
| Labeler Name: | Paddock Laboratories, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA040246 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20000901 | 
| Package NDC: | 0574-7226-12 | 
| Package Description: | 12 PACKET in 1 CARTON (0574-7226-12) > 1 SUPPOSITORY in 1 PACKET | 
| NDC Code | 0574-7226-12 | 
| Proprietary Name | Compro | 
| Package Description | 12 PACKET in 1 CARTON (0574-7226-12) > 1 SUPPOSITORY in 1 PACKET | 
| Product NDC | 0574-7226 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | PROCHLORPERAZINE | 
| Dosage Form Name | SUPPOSITORY | 
| Route Name | RECTAL | 
| Start Marketing Date | 20000901 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Paddock Laboratories, Inc. | 
| Substance Name | PROCHLORPERAZINE | 
| Strength Number | 25 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |