Product NDC: | 55910-050 |
Proprietary Name: | dg health Ibuprofen pm |
Non Proprietary Name: | diphenhydramine citrate and ibuprofen |
Active Ingredient(s): | 38; 200 mg/1; mg/1 & nbsp; diphenhydramine citrate and ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55910-050 |
Labeler Name: | Dolgencorp Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA079113 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100124 |
Package NDC: | 55910-050-60 |
Package Description: | 1 BOTTLE in 1 CARTON (55910-050-60) > 20 TABLET, COATED in 1 BOTTLE |
NDC Code | 55910-050-60 |
Proprietary Name | dg health Ibuprofen pm |
Package Description | 1 BOTTLE in 1 CARTON (55910-050-60) > 20 TABLET, COATED in 1 BOTTLE |
Product NDC | 55910-050 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | diphenhydramine citrate and ibuprofen |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20100124 |
Marketing Category Name | ANDA |
Labeler Name | Dolgencorp Inc |
Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
Strength Number | 38; 200 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |