MedPath

Folic Acid

FOLIC ACIDTABLETS, USP

Approved
Approval ID

3a1b39df-bc52-4ad7-87f6-ea77cac706f2

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 28, 2009

Manufacturers
FDA

Apace Packaging

DUNS: 361961142

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 Code15338-170
Application NumberNDA080680
Product Classification
M
Marketing Category
C73594
G
Generic Name
Folic Acid
Product Specifications
Route of AdministrationORAL
Effective DateDecember 31, 2009
FDA Product Classification

INGREDIENTS (5)

LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
FOLIC ACIDActive
Quantity: 1 mg in 1 1
Code: 935E97BOY8
Classification: ACTIB
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT

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