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Feverall Infants
Feverall Infants - 0472-1200-50 - (Acetaminophen)
Drug Information of Feverall Infants
| Product NDC: | 0472-1200 |
| Proprietary Name: | Feverall Infants |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 80 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Feverall Infants
| Product NDC: | 0472-1200 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA018337 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19800501 |
Package Information of Feverall Infants
| Package NDC: | 0472-1200-50 |
| Package Description: | 50 SUPPOSITORY in 1 BOTTLE (0472-1200-50) |
NDC Information of Feverall Infants
| NDC Code | 0472-1200-50 |
| Proprietary Name | Feverall Infants |
| Package Description | 50 SUPPOSITORY in 1 BOTTLE (0472-1200-50) |
| Product NDC | 0472-1200 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19800501 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 80 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
