| Product NDC: | 60258-050 |
| Proprietary Name: | APAP 500 |
| Non Proprietary Name: | Acetaminophen Oral Solution |
| Active Ingredient(s): | 500 mg/5mL & nbsp; Acetaminophen Oral Solution |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 60258-050 |
| Labeler Name: | Cypress Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19950615 |
| Package NDC: | 60258-050-08 |
| Package Description: | 237 mL in 1 BOTTLE (60258-050-08) |
| NDC Code | 60258-050-08 |
| Proprietary Name | APAP 500 |
| Package Description | 237 mL in 1 BOTTLE (60258-050-08) |
| Product NDC | 60258-050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen Oral Solution |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19950615 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Cypress Pharmaceutical, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |