Ceftriaxone Sodium
Ceftriaxone Sodium
Approved
Approval ID
473ab78d-5015-4a4a-8a2c-8f594b8de41d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 17, 2011
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ceftriaxone Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-352
Application NumberANDA065230
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ceftriaxone Sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 12, 2010
FDA Product Classification
INGREDIENTS (1)
CEFTRIAXONE SODIUMActive
Quantity: 1 g in 1 1
Code: 023Z5BR09K
Classification: ACTIM
Ceftriaxone Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code21695-202
Application NumberANDA065230
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ceftriaxone Sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 12, 2010
FDA Product Classification
INGREDIENTS (1)
CEFTRIAXONE SODIUMActive
Quantity: 500 mg in 1 1
Code: 023Z5BR09K
Classification: ACTIM