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ibuprofen
ibuprofen - 41250-995-83 - (Ibuprofen)
Drug Information of ibuprofen
| Product NDC: | 41250-995 |
| Proprietary Name: | ibuprofen |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 200 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: | 41250-995 |
| Labeler Name: | Meijer Distribution Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA077349 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19930401 |
Package Information of ibuprofen
| Package NDC: | 41250-995-83 |
| Package Description: | 225 TABLET, FILM COATED in 1 BOTTLE (41250-995-83) |
NDC Information of ibuprofen
| NDC Code | 41250-995-83 |
| Proprietary Name | ibuprofen |
| Package Description | 225 TABLET, FILM COATED in 1 BOTTLE (41250-995-83) |
| Product NDC | 41250-995 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19930401 |
| Marketing Category Name | ANDA |
| Labeler Name | Meijer Distribution Inc |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
