Home
>
National Drug Code (NDC)
>
Preferred Plus Ibuprofen 200
Preferred Plus Ibuprofen 200 - 61715-053-01 - (Ibuprofen)
Drug Information of Preferred Plus Ibuprofen 200
| Product NDC: | 61715-053 |
| Proprietary Name: | Preferred Plus Ibuprofen 200 |
| 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 Preferred Plus Ibuprofen 200
| Product NDC: | 61715-053 |
| Labeler Name: | Kinray |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130626 |
Package Information of Preferred Plus Ibuprofen 200
| Package NDC: | 61715-053-01 |
| Package Description: | 1 TABLET in 1 CARTON (61715-053-01) |
NDC Information of Preferred Plus Ibuprofen 200
| NDC Code | 61715-053-01 |
| Proprietary Name | Preferred Plus Ibuprofen 200 |
| Package Description | 1 TABLET in 1 CARTON (61715-053-01) |
| Product NDC | 61715-053 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130626 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kinray |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
