Product NDC: | 70253-291 |
Proprietary Name: | Ibuprofen |
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) |
Product NDC: | 70253-291 |
Labeler Name: | NASH-FINCH COMPANY |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075010 |
Marketing Category: | ANDA |
Start Marketing Date: | 19880524 |
Package NDC: | 70253-291-12 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (70253-291-12) > 100 TABLET in 1 BOTTLE, PLASTIC |
NDC Code | 70253-291-12 |
Proprietary Name | Ibuprofen |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (70253-291-12) > 100 TABLET in 1 BOTTLE, PLASTIC |
Product NDC | 70253-291 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19880524 |
Marketing Category Name | ANDA |
Labeler Name | NASH-FINCH COMPANY |
Substance Name | IBUPROFEN |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |