Loxapine
Loxapine Capsules, USP
Approved
Approval ID
9422b8f2-24cc-4387-acf1-f663dacb613c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 7, 2020
Manufacturers
FDA
ATLANTIC BIOLOGICALS CORP.
DUNS: 047437707
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Loxapine
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code17856-1397
Application NumberANDA090695
Product Classification
M
Marketing Category
C73584
G
Generic Name
Loxapine
Product Specifications
Route of AdministrationORAL
Effective DateAugust 5, 2020
FDA Product Classification
INGREDIENTS (17)
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
LOXAPINE SUCCINATEActive
Quantity: 50 mg in 1 1
Code: X59SG0MRYU
Classification: ACTIM
GELATINInactive
Code: 2G86QN327L
Classification: IACT
ANHYDROUS LACTOSEInactive
Code: 3SY5LH9PMK
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
POLACRILIN POTASSIUMInactive
Code: 0BZ5A00FQU
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
ALCOHOLInactive
Code: 3K9958V90M
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
SHELLACInactive
Code: 46N107B71O
Classification: IACT
ISOPROPYL ALCOHOLInactive
Code: ND2M416302
Classification: IACT
BUTYL ALCOHOLInactive
Code: 8PJ61P6TS3
Classification: IACT
AMMONIAInactive
Code: 5138Q19F1X
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT