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Pain Reliever PM Extra Strength
Pain Reliever PM Extra Strength - 37808-556-09 - (Acetaminophen, Diphenhydramine HCl)
Drug Information of Pain Reliever PM Extra Strength
| Product NDC: | 37808-556 |
| Proprietary Name: | Pain Reliever PM Extra Strength |
| Non Proprietary Name: | Acetaminophen, Diphenhydramine HCl |
| Active Ingredient(s): | 500; 25 mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pain Reliever PM Extra Strength
| Product NDC: | 37808-556 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20071217 |
Package Information of Pain Reliever PM Extra Strength
| Package NDC: | 37808-556-09 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (37808-556-09) > 20 CAPSULE in 1 BOTTLE, PLASTIC |
NDC Information of Pain Reliever PM Extra Strength
| NDC Code | 37808-556-09 |
| Proprietary Name | Pain Reliever PM Extra Strength |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (37808-556-09) > 20 CAPSULE in 1 BOTTLE, PLASTIC |
| Product NDC | 37808-556 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Diphenhydramine HCl |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20071217 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H E B |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
