ASCORBIC ACID
Approved
Approval ID
4eb6a932-244e-30c5-e054-00144ff8d46c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 29, 2017
Manufacturers
FDA
FLON LABORATORIES LLC
DUNS: 080592497
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 Code71414-115
Product Classification
G
Generic Name
ASCORBIC ACID
Product Specifications
Route of AdministrationINTRAMUSCULAR, SUBCUTANEOUS, INTRAVENOUS
Effective DateJune 29, 2017
FDA Product Classification
INGREDIENTS (5)
ASCORBIC ACIDActive
Quantity: 500 mg in 1 mL
Code: PQ6CK8PD0R
Classification: ACTIB
EDETATE DISODIUMInactive
Quantity: 0.25 mg in 1 mL
Code: 7FLD91C86K
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM BICARBONATEInactive
Code: 8MDF5V39QO
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT