Thiothixene
Thiothixene Capsules, USP
Approved
Approval ID
17dbfc4c-d62e-4efa-930d-29df7de69fa3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 27, 2010
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Thiothixene
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-161
Application NumberANDA071529
Product Classification
M
Marketing Category
C73584
G
Generic Name
Thiothixene
Product Specifications
Route of AdministrationORAL
Effective DateJuly 18, 2007
FDA Product Classification
INGREDIENTS (8)
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
GELATINInactive
Code: 2G86QN327L
Classification: IACT
THIOTHIXENEActive
Quantity: 5 mg in 1 1
Code: 7318FJ13YJ
Classification: ACTIB
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT