MedPath

Folic Acid

FOLIC ACID TABLETS, USP 1 mg Rx only

Approved
Approval ID

a5477715-93d0-4240-9a96-c4f47e99604c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 9, 2010

Manufacturers
FDA

Contract Pharmacy Services-PA

DUNS: 945429777

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 Code67046-216
Application NumberANDA040756
Product Classification
M
Marketing Category
C73584
G
Generic Name
Folic Acid
Product Specifications
Route of AdministrationORAL
Effective DateJune 4, 2010
FDA Product Classification

INGREDIENTS (5)

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

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Folic Acid - FDA Drug Approval Details