FOLIC ACID
FOLIC ACID TABLETS, USP
Approved
Approval ID
56ccdc1c-4f85-4b3a-b04b-3f06f37f816a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 3, 2018
Manufacturers
FDA
Central Texas Community Health Centers
DUNS: 079674019
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
FOLIC ACID
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code76413-163
Application NumberANDA040796
Product Classification
M
Marketing Category
C73584
G
Generic Name
FOLIC ACID
Product Specifications
Route of AdministrationORAL
Effective DateMay 31, 2016
FDA Product Classification
INGREDIENTS (5)
FOLIC ACIDActive
Quantity: 1 mg in 1 1
Code: 935E97BOY8
Classification: ACTIB
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT