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Ibuprofen
Ibuprofen - 21695-067-21 - (Ibuprofen)
Drug Information of Ibuprofen
| Product NDC: | 21695-067 |
| Proprietary Name: | Ibuprofen |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 600 mg/1 & nbsp; Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ibuprofen
| Product NDC: | 21695-067 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075682 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090610 |
Package Information of Ibuprofen
| Package NDC: | 21695-067-21 |
| Package Description: | 21 TABLET, FILM COATED in 1 BOTTLE (21695-067-21) |
NDC Information of Ibuprofen
| NDC Code | 21695-067-21 |
| Proprietary Name | Ibuprofen |
| Package Description | 21 TABLET, FILM COATED in 1 BOTTLE (21695-067-21) |
| Product NDC | 21695-067 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20090610 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | IBUPROFEN |
| Strength Number | 600 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
