| Product NDC: | 0472-1202 |
| Proprietary Name: | FeverALL Junior |
| Non Proprietary Name: | acetaminophen |
| Active Ingredient(s): | 325 mg/1 & nbsp; acetaminophen |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0472-1202 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA018337 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19800401 |
| Package NDC: | 0472-1202-06 |
| Package Description: | 6 SUPPOSITORY in 1 BOX (0472-1202-06) |
| NDC Code | 0472-1202-06 |
| Proprietary Name | FeverALL Junior |
| Package Description | 6 SUPPOSITORY in 1 BOX (0472-1202-06) |
| Product NDC | 0472-1202 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19800401 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |