Hydrochlorothiazide
HYDROCHLOROTHIAZIDE TABLETS USP
Approved
Approval ID
fe6200cc-3182-473c-a90a-a8caa2fb2818
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 16, 2010
Manufacturers
FDA
Contract Pharmacy Services-PA
DUNS: 945429777
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Hydrochlorothiazide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code67046-276
Application NumberANDA040702
Product Classification
M
Marketing Category
C73584
G
Generic Name
Hydrochlorothiazide
Product Specifications
Route of AdministrationORAL
Effective DateApril 8, 2009
FDA Product Classification
INGREDIENTS (1)
HydrochlorothiazideActive
Quantity: 50 mg in 1 1
Code: 0J48LPH2TH
Classification: ACTIB
Hydrochlorothiazide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code67046-275
Application NumberANDA040702
Product Classification
M
Marketing Category
C73584
G
Generic Name
Hydrochlorothiazide
Product Specifications
Route of AdministrationORAL
Effective DateApril 8, 2009
FDA Product Classification
INGREDIENTS (1)
HydrochlorothiazideActive
Quantity: 25 mg in 1 1
Code: 0J48LPH2TH
Classification: ACTIB