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
NDC Product Code66336-907
Application NumberANDA040833
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateFebruary 6, 2012
Generic NameErgocalciferol
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