Product NDC: | 62011-0024 |
Proprietary Name: | Extra Strength Acetaminophen PM |
Non Proprietary Name: | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62011-0024 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120409 |
Package NDC: | 62011-0024-1 |
Package Description: | 1 BOTTLE in 1 BOX (62011-0024-1) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Code | 62011-0024-1 |
Proprietary Name | Extra Strength Acetaminophen PM |
Package Description | 1 BOTTLE in 1 BOX (62011-0024-1) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE |
Product NDC | 62011-0024 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20120409 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | McKesson |
Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
Strength Number | 500; 25 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |