NDC 51808-220

Sulfur Colloid

Sulfur Colloid

Sulfur Colloid is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Anazaohealth Corporation. The primary component is Gelatin.

Product ID51808-220_7c1f657a-07f0-4f9f-9552-1688174e2130
NDC51808-220
Product TypeHuman Prescription Drug
Proprietary NameSulfur Colloid
Generic NameSulfur Colloid
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2012-07-01
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameAnazaoHealth Corporation
Substance NameGELATIN
Active Ingredient Strength5 mg/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 51808-220-01

1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-220-01)
Marketing Start Date2012-07-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51808-220-01 [51808022001]

Sulfur Colloid INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-07-01
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
GELATIN4.5 mg/1

OpenFDA Data

SPL SET ID:26dde4a4-9bb1-4adc-a5f2-fb44e42e5c15
Manufacturer
UNII

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