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Acetaminophen
Acetaminophen - 54868-5624-0 - (Acetaminophen)
Drug Information of Acetaminophen
| Product NDC: | 54868-5624 |
| Proprietary Name: | Acetaminophen |
| 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) |
Labeler Information of Acetaminophen
| Product NDC: | 54868-5624 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA018060 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060629 |
Package Information of Acetaminophen
| Package NDC: | 54868-5624-0 |
| Package Description: | 12 SUPPOSITORY in 1 BOX (54868-5624-0) |
NDC Information of Acetaminophen
| NDC Code | 54868-5624-0 |
| Proprietary Name | Acetaminophen |
| Package Description | 12 SUPPOSITORY in 1 BOX (54868-5624-0) |
| Product NDC | 54868-5624 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 20060629 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 120 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
