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Pain Relief
Pain Relief - 59726-117-10 - (Ibuprofen)
Drug Information of Pain Relief
| Product NDC: | 59726-117 |
| Proprietary Name: | Pain Relief |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 200 mg/1 & nbsp; Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pain Relief
| Product NDC: | 59726-117 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079174 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120813 |
Package Information of Pain Relief
| Package NDC: | 59726-117-10 |
| Package Description: | 10 TABLET, COATED in 1 VIAL (59726-117-10) |
NDC Information of Pain Relief
| NDC Code | 59726-117-10 |
| Proprietary Name | Pain Relief |
| Package Description | 10 TABLET, COATED in 1 VIAL (59726-117-10) |
| Product NDC | 59726-117 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120813 |
| Marketing Category Name | ANDA |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
