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Childrens Acetaminophen
Childrens Acetaminophen - 68094-650-62 - (Acetaminophen)
Drug Information of Childrens Acetaminophen
| Product NDC: | 68094-650 |
| Proprietary Name: | Childrens Acetaminophen |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 650 mg/20.3mL & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Acetaminophen
| Product NDC: | 68094-650 |
| Labeler Name: | Precision Dose Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080321 |
Package Information of Childrens Acetaminophen
| Package NDC: | 68094-650-62 |
| Package Description: | 3 TRAY in 1 CASE (68094-650-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 20.3 mL in 1 CUP, UNIT-DOSE (68094-650-59) |
NDC Information of Childrens Acetaminophen
| NDC Code | 68094-650-62 |
| Proprietary Name | Childrens Acetaminophen |
| Package Description | 3 TRAY in 1 CASE (68094-650-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 20.3 mL in 1 CUP, UNIT-DOSE (68094-650-59) |
| Product NDC | 68094-650 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20080321 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Precision Dose Inc. |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/20.3mL |
| Pharmaceutical Classes |
