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Ibuprofen (NSAID)
Ibuprofen (NSAID) - 21695-065-30 - (Ibuprofen (NSAID))
Drug Information of Ibuprofen (NSAID)
| Product NDC: | 21695-065 |
| Proprietary Name: | Ibuprofen (NSAID) |
| Non Proprietary Name: | Ibuprofen (NSAID) |
| Active Ingredient(s): | 200 mg/1 & nbsp; Ibuprofen (NSAID) |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ibuprofen (NSAID)
| Product NDC: | 21695-065 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA071333 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091216 |
Package Information of Ibuprofen (NSAID)
| Package NDC: | 21695-065-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (21695-065-30) |
NDC Information of Ibuprofen (NSAID)
| NDC Code | 21695-065-30 |
| Proprietary Name | Ibuprofen (NSAID) |
| Package Description | 30 TABLET in 1 BOTTLE (21695-065-30) |
| Product NDC | 21695-065 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen (NSAID) |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091216 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
