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Tylenol
Tylenol - 55154-1918-0 - (Acetaminophen)
Drug Information of Tylenol
| Product NDC: | 55154-1918 |
| Proprietary Name: | Tylenol |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 325 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tylenol
| Product NDC: | 55154-1918 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110606 |
Package Information of Tylenol
| Package NDC: | 55154-1918-0 |
| Package Description: | 10 BLISTER PACK in 1 BAG (55154-1918-0) > 1 TABLET in 1 BLISTER PACK |
NDC Information of Tylenol
| NDC Code | 55154-1918-0 |
| Proprietary Name | Tylenol |
| Package Description | 10 BLISTER PACK in 1 BAG (55154-1918-0) > 1 TABLET in 1 BLISTER PACK |
| Product NDC | 55154-1918 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110606 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cardinal Health |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
