Ascorbic Acid
Ascorbic box of 10 revised
Approved
Approval ID
1ac7a17e-75d0-4444-e054-00144ff88e88
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 22, 2017
Manufacturers
FDA
Raw Materials International Overseas LLC
DUNS: 079829477
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ascorbic Acid
PRODUCT DETAILS
NDC Product Code69877-017
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationSUBCUTANEOUS, INTRAVENOUS, INTRAMUSCULAR
Effective DateFebruary 22, 2017
Generic NameAscorbic Acid
INGREDIENTS (5)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
EDETATE DISODIUMInactive
Quantity: 0.25 mg in 1 mL
Code: 7FLD91C86K
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
ASCORBIC ACIDActive
Quantity: 500 mg in 1 mL
Code: PQ6CK8PD0R
Classification: ACTIB