NDC 72689-0023

KIMITE

Scopolamine

KIMITE is a Topical Patch, Extended Release in the Human Otc Drug category. It is labeled and distributed by Oasis Trading. The primary component is Scopolamine.

Product ID72689-0023_7ccd63d8-5cb8-4142-e053-2991aa0a0531
NDC72689-0023
Product TypeHuman Otc Drug
Proprietary NameKIMITE
Generic NameScopolamine
Dosage FormPatch, Extended Release
Route of AdministrationTOPICAL
Marketing Start Date2018-11-15
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameOASIS TRADING
Substance NameSCOPOLAMINE
Active Ingredient Strength2 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 72689-0023-1

2 PATCH, EXTENDED RELEASE in 1 BOX (72689-0023-1)
Marketing Start Date2018-11-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72689-0023-1 [72689002301]

KIMITE PATCH, EXTENDED RELEASE
Marketing Categoryunapproved drug other
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-11-16
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SCOPOLAMINE1.5 mg/1

OpenFDA Data

SPL SET ID:7ccd63d8-5cb7-4142-e053-2991aa0a0531
Manufacturer
UNII

NDC Crossover Matching brand name "KIMITE" or generic name "Scopolamine"

NDCBrand NameGeneric Name
72689-0023KIMITEScopolamine
0378-6470Scopolaminescopolamine
0591-2258scopolaminescopolamine
50090-5349Scopolaminescopolamine
50742-505ScopolamineScopolamine
0067-4345Transderm Scopscopolamine
0067-4346Transderm Scopscopolamine
66758-208Transderm Scopscopolamine

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