Product NDC: | 0472-1201 |
Proprietary Name: | FeverALL 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: | 0472-1201 |
Labeler Name: | Actavis Mid Atlantic LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA018337 |
Marketing Category: | ANDA |
Start Marketing Date: | 19800401 |
Package NDC: | 0472-1201-06 |
Package Description: | 6 SUPPOSITORY in 1 BOX (0472-1201-06) |
NDC Code | 0472-1201-06 |
Proprietary Name | FeverALL Children |
Package Description | 6 SUPPOSITORY in 1 BOX (0472-1201-06) |
Product NDC | 0472-1201 |
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 | 120 |
Strength Unit | mg/1 |
Pharmaceutical Classes |