Product NDC: | 25000-133 |
Proprietary Name: | IBUPROFEN |
Non Proprietary Name: | ibuprofen |
Active Ingredient(s): | 200 mg/1 & nbsp; ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 25000-133 |
Labeler Name: | Marksans Pharma Limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA079205 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110509 |
Package NDC: | 25000-133-18 |
Package Description: | 4 BAG in 1 BOX (25000-133-18) > 2500 CAPSULE, LIQUID FILLED in 1 BAG |
NDC Code | 25000-133-18 |
Proprietary Name | IBUPROFEN |
Package Description | 4 BAG in 1 BOX (25000-133-18) > 2500 CAPSULE, LIQUID FILLED in 1 BAG |
Product NDC | 25000-133 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ibuprofen |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20110509 |
Marketing Category Name | ANDA |
Labeler Name | Marksans Pharma Limited |
Substance Name | IBUPROFEN |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |