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Cedaprin
Cedaprin - 0498-7500-50 - (Ibuprofen)
Drug Information of Cedaprin
| Product NDC: | 0498-7500 |
| Proprietary Name: | Cedaprin |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 200 mg/1 & nbsp; Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cedaprin
| Product NDC: | 0498-7500 |
| Labeler Name: | North Safety Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079129 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120307 |
Package Information of Cedaprin
| Package NDC: | 0498-7500-50 |
| Package Description: | 250 BOX in 1 BOX (0498-7500-50) > 125 BOX in 1 BOX (0498-7500-25) > 50 PACKET in 1 BOX (0498-7500-10) > 2 TABLET in 1 PACKET (0498-7500-01) |
NDC Information of Cedaprin
| NDC Code | 0498-7500-50 |
| Proprietary Name | Cedaprin |
| Package Description | 250 BOX in 1 BOX (0498-7500-50) > 125 BOX in 1 BOX (0498-7500-25) > 50 PACKET in 1 BOX (0498-7500-10) > 2 TABLET in 1 PACKET (0498-7500-01) |
| Product NDC | 0498-7500 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120307 |
| Marketing Category Name | ANDA |
| Labeler Name | North Safety Products LLC |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
