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FeverALL Adults
FeverALL Adults - 0472-1203-50 - (acetaminophen)
Drug Information of FeverALL Adults
| Product NDC: | 0472-1203 |
| Proprietary Name: | FeverALL Adults |
| Non Proprietary Name: | acetaminophen |
| Active Ingredient(s): | 650 mg/1 & nbsp; acetaminophen |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FeverALL Adults
| Product NDC: | 0472-1203 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA018337 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19800401 |
Package Information of FeverALL Adults
| Package NDC: | 0472-1203-50 |
| Package Description: | 50 SUPPOSITORY in 1 BOX (0472-1203-50) |
NDC Information of FeverALL Adults
| NDC Code | 0472-1203-50 |
| Proprietary Name | FeverALL Adults |
| Package Description | 50 SUPPOSITORY in 1 BOX (0472-1203-50) |
| Product NDC | 0472-1203 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19800401 |
| Marketing Category Name | NDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
