Product NDC: | 55910-217 |
Proprietary Name: | Dg Health pain reliever |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 650 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55910-217 |
Labeler Name: | Dolgencorp, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075077 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100105 |
Package NDC: | 55910-217-71 |
Package Description: | 1 BOTTLE in 1 CARTON (55910-217-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
NDC Code | 55910-217-71 |
Proprietary Name | Dg Health pain reliever |
Package Description | 1 BOTTLE in 1 CARTON (55910-217-71) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
Product NDC | 55910-217 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20100105 |
Marketing Category Name | ANDA |
Labeler Name | Dolgencorp, LLC |
Substance Name | ACETAMINOPHEN |
Strength Number | 650 |
Strength Unit | mg/1 |
Pharmaceutical Classes |