Doxycycline
DOXYCYCLINE HYCLATETABLETS, USP
Approved
Approval ID
6adc5bb0-69a5-4c9f-b569-1eee446afcd2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 3, 2011
Manufacturers
FDA
Legacy Pharmaceutical Packaging
DUNS: 143213275
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Doxycycline hyclate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68645-021
Application NumberANDA065095
Product Classification
M
Marketing Category
C73584
G
Generic Name
Doxycycline hyclate
Product Specifications
Route of AdministrationORAL
Effective DateMay 3, 2011
FDA Product Classification
INGREDIENTS (5)
DOXYCYCLINE HYCLATEActive
Quantity: 100 mg in 1 1
Code: 19XTS3T51U
Classification: ACTIB
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
COLLOIDAL SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT