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Acetaminophen
Acetaminophen - 0121-0657-21 - (Acetaminophen)
Drug Information of Acetaminophen
| Product NDC: | 0121-0657 |
| Proprietary Name: | Acetaminophen |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 160 mg/5mL & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acetaminophen
| Product NDC: | 0121-0657 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20070801 |
Package Information of Acetaminophen
| Package NDC: | 0121-0657-21 |
| Package Description: | 10 TRAY in 1 CASE (0121-0657-21) > 10 CUP, UNIT-DOSE in 1 TRAY > 20.3 mL in 1 CUP, UNIT-DOSE |
NDC Information of Acetaminophen
| NDC Code | 0121-0657-21 |
| Proprietary Name | Acetaminophen |
| Package Description | 10 TRAY in 1 CASE (0121-0657-21) > 10 CUP, UNIT-DOSE in 1 TRAY > 20.3 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-0657 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20070801 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Pharmaceutical Associates, Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 160 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
