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APROFEN
APROFEN - 46084-021-22 - (IBUPROFEN)
Drug Information of APROFEN
| Product NDC: | 46084-021 |
| Proprietary Name: | APROFEN |
| 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 APROFEN
| Product NDC: | 46084-021 |
| Labeler Name: | A P J Laboratories Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130221 |
Package Information of APROFEN
| Package NDC: | 46084-021-22 |
| Package Description: | 50 TABLET in 1 BLISTER PACK (46084-021-22) |
NDC Information of APROFEN
| NDC Code | 46084-021-22 |
| Proprietary Name | APROFEN |
| Package Description | 50 TABLET in 1 BLISTER PACK (46084-021-22) |
| Product NDC | 46084-021 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130221 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | A P J Laboratories Limited |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
