Product NDC: | 62011-0016 |
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: | 62011-0016 |
Labeler Name: | McKesson (Health Mart) |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA078682 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120409 |
Package NDC: | 62011-0016-1 |
Package Description: | 1 BOTTLE in 1 BOX (62011-0016-1) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Code | 62011-0016-1 |
Proprietary Name | IBUPROFEN |
Package Description | 1 BOTTLE in 1 BOX (62011-0016-1) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE |
Product NDC | 62011-0016 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | IBUPROFEN |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20120409 |
Marketing Category Name | ANDA |
Labeler Name | McKesson (Health Mart) |
Substance Name | IBUPROFEN |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |