NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2413Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2413Add 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 NDC11-digit (billing)PackageCopy
72162-2413-0721622413001000 TABLET in 1 BOTTLE (72162-2413-0)Marketed from Oct 31, 2024
72162-2413-172162241301100 TABLET in 1 BOTTLE (72162-2413-1)Marketed from Oct 31, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202437
Marketing start
Listing expires
Identifiers
Product ID 72162-2413_7fee2a67-d0a3-4a68-b54f-4eb7ebd63f4dSPL ID 7fee2a67-d0a3-4a68-b54f-4eb7ebd63f4dSPL set ID f4ede23e-f091-46cb-b120-772ee71b8cb3RxCUI 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

N472162241300 followed by a unit qualifier and the quantity

Package 72162-2413-00. 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 .

Indications (excerpt from the label)

INDICATIONS & USAGE Folic acid, USP 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 202437

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

FDA NDC Directory listings under ANDA 202437
ProductStrengthForm · routeLabelerProduct NDC
Folic AcidFolic acid 1 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8827
Folic AcidFolic acid 1 mg/1TabletOralCoupler LLC67046-1449
Folic AcidFolic acid 1 mg/1TabletOralCadila Pharmaceuticals Limited71209-007
Folic AcidFolic acid 1 mg/1TabletOralREMEDYREPACK INC.70518-4338
Folic AcidFolic acid 1 mg/1TabletOralModavar Pharmaceuticals LLC72241-050
Folic AcidFolic acid 1 mg/1TabletOralBryant Ranch Prepack71335-2547

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