Folic Acid NDC 70752-231

NDC codes

FDA NDC Directory

Product NDC (as listed)70752-231Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70752-0231Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
70752-231-10	70752023110	100 TABLET in 1 BOTTLE (70752-231-10)Marketed from Jul 10, 2023
70752-231-11	70752023111	1000 TABLET in 1 BOTTLE (70752-231-11)Marketed from Jul 10, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Folic Acid
Generic name (nonproprietary): folic acid
Active ingredients: Folic acid — 1 mg/1
Dosage form: Tablet
Route: Oral
Labeler: QUAGEN PHARMACEUTICALS LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 091145
Marketing start: Jul 10, 2023
Listing expires: Dec 31, 2027
Identifiers: Product ID 70752-231_067af2c9-3769-40d4-a991-217390ece384SPL ID 067af2c9-3769-40d4-a991-217390ece384SPL set ID 354366ea-3702-4706-9fc0-0244b7278bd8RxCUI 310410UNII 935E97BOY8

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470752023110 followed by a unit qualifier and the quantity

Package 70752-0231-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective May 20, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Folic acid is effective in the treatment of megaloblastic anemias due to a deficiency of folic acid (as may be seen in tropical or nontropical sprue) and in anemias of nutritional origin, pregnancy, infancy, or childhood.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 091145

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 091145
Product	Strength	Form · route	Labeler	Product NDC
Folic Acid	Folic acid 1 mg/1	TabletOral	Bryant Ranch Prepack	72162-2556
Folic Acid	Folic acid 1 mg/1	TabletOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8589