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Acetaminophen PM
Acetaminophen PM - 57344-095-02 - (Acetaminophen and DIPHENHYDRAMINE HYDROCHLORIDE)
Drug Information of Acetaminophen PM
| Product NDC: | 57344-095 |
| Proprietary Name: | Acetaminophen PM |
| 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, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acetaminophen PM
| Product NDC: | 57344-095 |
| Labeler Name: | AAA Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part338 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121213 |
Package Information of Acetaminophen PM
| Package NDC: | 57344-095-02 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (57344-095-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
NDC Information of Acetaminophen PM
| NDC Code | 57344-095-02 |
| Proprietary Name | Acetaminophen PM |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (57344-095-02) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
| Product NDC | 57344-095 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen and DIPHENHYDRAMINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121213 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | AAA Pharmaceutical, Inc. |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
| Strength Number | 500; 25 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
