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Ibuprofen
Ibuprofen - 17856-5309-5 - (Ibuprofen)
Drug Information of Ibuprofen
| Product NDC: | 17856-5309 |
| Proprietary Name: | 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) |
Labeler Information of Ibuprofen
| Product NDC: | 17856-5309 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074937 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990207 |
Package Information of Ibuprofen
| Package NDC: | 17856-5309-5 |
| Package Description: | 5 mL in 1 CUP (17856-5309-5) |
NDC Information of Ibuprofen
| NDC Code | 17856-5309-5 |
| Proprietary Name | Ibuprofen |
| Package Description | 5 mL in 1 CUP (17856-5309-5) |
| Product NDC | 17856-5309 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19990207 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | IBUPROFEN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
