Ergocalciferol
Approved
Approval ID
0525e04f-91b7-4d75-8ff9-a6fb5705d993
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 6, 2012
Manufacturers
FDA
Dispensing Solutions, Inc.
DUNS: 066070785
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ergocalciferol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code66336-907
Application NumberANDA040833
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ergocalciferol
Product Specifications
Route of AdministrationORAL
Effective DateFebruary 6, 2012
FDA Product Classification
INGREDIENTS (7)
D&C Yellow No. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
GelatinInactive
Code: 2G86QN327L
Classification: IACT
Soybean OilInactive
Code: 241ATL177A
Classification: IACT
ErgocalciferolActive
Quantity: 1.25 mg in 1 1
Code: VS041H42XC
Classification: ACTIB
FD&C Blue No. 1Inactive
Code: H3R47K3TBD
Classification: IACT
GlycerinInactive
Code: PDC6A3C0OX
Classification: IACT
WaterInactive
Code: 059QF0KO0R
Classification: IACT