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Extra Strength Pain Relief PM
Extra Strength Pain Relief PM - 59726-360-50 - (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE)
Drug Information of Extra Strength Pain Relief PM
| Product NDC: | 59726-360 |
| Proprietary Name: | Extra Strength Pain Relief 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) |
Labeler Information of Extra Strength Pain Relief PM
| Product NDC: | 59726-360 |
| Labeler Name: | P and L Development of New York Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110902 |
Package Information of Extra Strength Pain Relief PM
| Package NDC: | 59726-360-50 |
| Package Description: | 1 BOTTLE in 1 BOX (59726-360-50) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Information of Extra Strength Pain Relief PM
| NDC Code | 59726-360-50 |
| Proprietary Name | Extra Strength Pain Relief PM |
| Package Description | 1 BOTTLE in 1 BOX (59726-360-50) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 59726-360 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20110902 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | P and L Development of New York Corporation |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
