Folic acid NDC 62135-210

NDC codes

FDA NDC Directory

Product NDC (as listed)62135-210Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62135-0210Add 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
62135-210-01	62135021001	100 TABLET in 1 BOTTLE (62135-210-01)Marketed from May 30, 2019
62135-210-05	62135021005	500 TABLET in 1 BOTTLE (62135-210-05)Marketed from Mar 9, 2022
62135-210-10	62135021010	1000 TABLET in 1 BOTTLE (62135-210-10)Marketed from May 30, 2019
62135-210-72	62135021072	1800 TABLET in 1 BOTTLE (62135-210-72)Marketed from Mar 3, 2022
62135-210-90	62135021090	90 TABLET in 1 BOTTLE (62135-210-90)Marketed from Mar 3, 2022
62135-210-97	62135021097	3000 TABLET in 1 BOTTLE (62135-210-97)Marketed from May 30, 2019

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: Chartwell RX, LLC.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090035
Marketing start: May 30, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 62135-210_2589605c-12b7-ed10-e063-6294a90ab52bSPL ID 2589605c-12b7-ed10-e063-6294a90ab52bSPL set ID 9a533666-8906-438e-adf7-11bb162ecb63RxCUI 310410UNII 935E97BOY8UPC 0362135210014, 0362135210908, 0362135210724, 0362135210052

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

N462135021001 followed by a unit qualifier and the quantity

Package 62135-0210-01. 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 Oct 28, 2024.

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 090035

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

FDA NDC Directory listings under ANDA 090035
Product	Strength	Form · route	Labeler	Product NDC
Folic acid	Folic acid 1 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-545