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Acetaminophen
Acetaminophen - 17714-012-01 - (Acetaminophen)
Drug Information of Acetaminophen
| Product NDC: | 17714-012 |
| Proprietary Name: | Acetaminophen |
| 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 Acetaminophen
| Product NDC: | 17714-012 |
| Labeler Name: | Advance Pharmaceutical Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19890205 |
Package Information of Acetaminophen
| Package NDC: | 17714-012-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (17714-012-01) |
NDC Information of Acetaminophen
| NDC Code | 17714-012-01 |
| Proprietary Name | Acetaminophen |
| Package Description | 100 TABLET in 1 BOTTLE (17714-012-01) |
| Product NDC | 17714-012 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19890205 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Advance Pharmaceutical Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 325 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
