Product NDC: | 54868-5623 |
Proprietary Name: | Ibuprofen |
Non Proprietary Name: | Ibuprofen |
Active Ingredient(s): | 100 mg/1 & nbsp; Ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5623 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA076359 |
Marketing Category: | ANDA |
Start Marketing Date: | 20071016 |
Package NDC: | 54868-5623-0 |
Package Description: | 1 BOTTLE in 1 CARTON (54868-5623-0) > 24 TABLET, CHEWABLE in 1 BOTTLE |
NDC Code | 54868-5623-0 |
Proprietary Name | Ibuprofen |
Package Description | 1 BOTTLE in 1 CARTON (54868-5623-0) > 24 TABLET, CHEWABLE in 1 BOTTLE |
Product NDC | 54868-5623 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20071016 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | IBUPROFEN |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes |