| Product NDC: | 68788-0426 |
| Proprietary Name: | Acetaminophen for Children |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 120 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68788-0426 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA070607 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101028 |
| Package NDC: | 68788-0426-1 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (68788-0426-1) > 6 SUPPOSITORY in 1 BLISTER PACK |
| NDC Code | 68788-0426-1 |
| Proprietary Name | Acetaminophen for Children |
| Package Description | 2 BLISTER PACK in 1 CARTON (68788-0426-1) > 6 SUPPOSITORY in 1 BLISTER PACK |
| Product NDC | 68788-0426 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 20101028 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |