Desmopressin Acetate
Desmporessin Acetate Tablets 0.1 mg, 0.2 mg
Approved
Approval ID
c04357fd-478a-4909-b098-ae6710be071c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 4, 2023
Manufacturers
FDA
BluePoint Laboratories
DUNS: 985523874
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
desmopressin acetate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68001-575
Application NumberANDA077414
Product Classification
M
Marketing Category
C73584
G
Generic Name
desmopressin acetate
Product Specifications
Route of AdministrationORAL
Effective DateAugust 4, 2023
FDA Product Classification
INGREDIENTS (4)
LACTOSE, UNSPECIFIED FORMInactive
Code: J2B2A4N98G
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
DESMOPRESSIN ACETATEActive
Quantity: 0.2 mg in 1 1
Code: XB13HYU18U
Classification: ACTIB
desmopressin acetate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68001-574
Application NumberANDA077414
Product Classification
M
Marketing Category
C73584
G
Generic Name
desmopressin acetate
Product Specifications
Route of AdministrationORAL
Effective DateAugust 4, 2023
FDA Product Classification
INGREDIENTS (4)
LACTOSE, UNSPECIFIED FORMInactive
Code: J2B2A4N98G
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
DESMOPRESSIN ACETATEActive
Quantity: 0.1 mg in 1 1
Code: XB13HYU18U
Classification: ACTIB