| Product NDC: | 0404-0716 |
| Proprietary Name: | Henry Schein Acetaminophen |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0404-0716 |
| Labeler Name: | Henry Schein, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20081230 |
| Package NDC: | 0404-0716-99 |
| Package Description: | 2 TABLET, FILM COATED in 1 PACKET (0404-0716-99) |
| NDC Code | 0404-0716-99 |
| Proprietary Name | Henry Schein Acetaminophen |
| Package Description | 2 TABLET, FILM COATED in 1 PACKET (0404-0716-99) |
| Product NDC | 0404-0716 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Henry Schein, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |