Product NDC: | 68094-494 |
Proprietary Name: | Childrens Ibuprofen |
Non Proprietary Name: | Ibuprofen |
Active Ingredient(s): | 100 mg/5mL & nbsp; Ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68094-494 |
Labeler Name: | Precision Dose Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA074937 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040413 |
Package NDC: | 68094-494-61 |
Package Description: | 10 TRAY in 1 CASE (68094-494-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-494-59) |
NDC Code | 68094-494-61 |
Proprietary Name | Childrens Ibuprofen |
Package Description | 10 TRAY in 1 CASE (68094-494-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-494-59) |
Product NDC | 68094-494 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20040413 |
Marketing Category Name | ANDA |
Labeler Name | Precision Dose Inc. |
Substance Name | IBUPROFEN |
Strength Number | 100 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |