NDC 58809-444

Vanapain PM

Choline Salicylate, Diphenhydramine Hydrochloride

Vanapain PM is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Gm Pharmaceuticals, Inc.. The primary component is Choline Salicylate; Diphenhydramine Hydrochloride.

Product ID58809-444_1edb4799-f2db-1737-e054-00144ff8d46c
NDC58809-444
Product TypeHuman Otc Drug
Proprietary NameVanapain PM
Generic NameCholine Salicylate, Diphenhydramine Hydrochloride
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2013-10-28
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameGM Pharmaceuticals, Inc.
Substance NameCHOLINE SALICYLATE; DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength870 mg/57mL; mg/57mL
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 58809-444-60

57 mL in 1 BOTTLE, PLASTIC (58809-444-60)
Marketing Start Date2013-10-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58809-444-60 [58809044460]

Vanapain PM LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-10-28
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CHOLINE SALICYLATE870 mg/57mL

OpenFDA Data

SPL SET ID:e09fd05f-9e88-4f91-a227-f7718531f3f2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1664658

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