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XL-DOL
XL-DOL - 63654-500-20 - (acetaminophen)
Drug Information of XL-DOL
| Product NDC: | 63654-500 |
| Proprietary Name: | XL-DOL |
| Non Proprietary Name: | acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of XL-DOL
| Product NDC: | 63654-500 |
| Labeler Name: | Selder, S.A. de C.V. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111115 |
Package Information of XL-DOL
| Package NDC: | 63654-500-20 |
| Package Description: | 20 TABLET in 1 BOX (63654-500-20) |
NDC Information of XL-DOL
| NDC Code | 63654-500-20 |
| Proprietary Name | XL-DOL |
| Package Description | 20 TABLET in 1 BOX (63654-500-20) |
| Product NDC | 63654-500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111115 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Selder, S.A. de C.V. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
