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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69877-017
Product Classification
G
Generic Name
Ascorbic Acid
Product Specifications
Route of AdministrationSUBCUTANEOUS, INTRAVENOUS, INTRAMUSCULAR
Effective DateFebruary 22, 2017
FDA Product Classification
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