Product NDC: | 61245-083 |
Proprietary Name: | Conney Ibuprofen |
Non Proprietary Name: | Ibuprofen |
Active Ingredient(s): | 200 mg/1 & nbsp; Ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61245-083 |
Labeler Name: | Conney Safety Products, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075139 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111114 |
Package NDC: | 61245-083-13 |
Package Description: | 250 PACKET in 1 BOX, UNIT-DOSE (61245-083-13) > 2 TABLET, FILM COATED in 1 PACKET |
NDC Code | 61245-083-13 |
Proprietary Name | Conney Ibuprofen |
Package Description | 250 PACKET in 1 BOX, UNIT-DOSE (61245-083-13) > 2 TABLET, FILM COATED in 1 PACKET |
Product NDC | 61245-083 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20111114 |
Marketing Category Name | ANDA |
Labeler Name | Conney Safety Products, LLC |
Substance Name | IBUPROFEN |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes |