Product NDC: | 65437-041 |
Proprietary Name: | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
Non Proprietary Name: | ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65437-041 |
Labeler Name: | HIMPRIT PHARMACHEM PVT LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100701 |
Package NDC: | 65437-041-31 |
Package Description: | 1 BAG in 1 DRUM (65437-041-31) > 31000 TABLET, FILM COATED in 1 BAG |
NDC Code | 65437-041-31 |
Proprietary Name | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE |
Package Description | 1 BAG in 1 DRUM (65437-041-31) > 31000 TABLET, FILM COATED in 1 BAG |
Product NDC | 65437-041 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ACETAMINOPHEN and DIPHENHYDRAMINE HYDROCHLORIDE |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20100701 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | HIMPRIT PHARMACHEM PVT LTD |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 500; 25 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |