NDC codes

FDA NDC Directory
Product NDC (as listed)71205-913Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71205-0913Add 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
71205-913-007120509130071205091300100 TABLET in 1 BOTTLE (71205-913-00)Marketed from Jul 15, 2021
71205-913-1171205091311712050913111000 TABLET in 1 BOTTLE (71205-913-11)Marketed from Jul 15, 2021
71205-913-30712050913307120509133030 TABLET in 1 BOTTLE (71205-913-30)Marketed from Jul 15, 2021
71205-913-557120509135571205091355500 TABLET in 1 BOTTLE (71205-913-55)Marketed from Jul 15, 2021
71205-913-60712050913607120509136060 TABLET in 1 BOTTLE (71205-913-60)Marketed from Jul 15, 2021
71205-913-90712050913907120509139090 TABLET in 1 BOTTLE (71205-913-90)Marketed from Jul 15, 2021

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
Proficient Rx LPNDC labeler code 71205
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040796
Marketing start
Listing expires
Identifiers
Product ID 71205-913_b78a6505-03e7-4f18-89ef-737f807df7c2SPL ID b78a6505-03e7-4f18-89ef-737f807df7c2SPL set ID 607d23e8-21ef-4d73-88f1-990cf267d22eRxCUI 310410UNII 935E97BOY8UPC 0371205913304

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

N471205091300 followed by a unit qualifier and the quantity

Package 71205-0913-00. 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 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)

About NDC 71205-913

What is NDC 71205-913?
71205-913 is the product NDC for Folic Acid, Folic acid 1 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 6 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Folic Acid.
What is the active ingredient?
Folic acid.
Who is the labeler?
Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Folic Acid?
56 other product NDCs are listed under this name. See all Folic Acid NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Folic Acid NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Folic AcidFolic acid 1 mg/1TabletOralREMEDYREPACK INC.70518-475670518-4756-00
Folic AcidFolic acid 1 mg/1TabletOralUnit Dose Solutions, Inc.87441-03287441-0032-01
Folic AcidFolic acid 1 mg/1TabletOralCoupler LLC67046-071967046-0719-03
Folic AcidFolic acid 1 mg/5mLSolutionOralAyurax, LLC73308-50173308-0501-75
Folic AcidFolic acid 1 mg/1TabletOralREMEDYREPACK INC.70518-445970518-4459-0070518-4459-01
Folic AcidFolic acid 1 mg/1TabletOralREMEDYREPACK INC.70518-433870518-4338-00
Folic AcidFolic acid 1 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-882768788-8827-0168788-8827-0368788-8827-06+1 more
Folic AcidFolic acid 1 mg/1TabletOralCoupler LLC67046-144967046-1449-03
Folic AcidFolic acid 1 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-855768788-8557-0168788-8557-0368788-8557-06+1 more
Folic AcidFolic acid 1 mg/1TabletOralNorthwind Health Company, LLC82868-00482868-0004-30

All 57 Folic Acid NDCs

Other NDCs under ANDA 040796

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

FDA NDC Directory listings under ANDA 040796
ProductStrengthForm · routeLabelerProduct NDC
Folic AcidFolic acid 1 mg/1TabletOralNuCare Pharmaceuticals, Inc.66267-217
Folic AcidFolic acid 1 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4602
Folic AcidFolic acid 1 mg/1TabletOralLeading Pharma, LLC69315-127
Folic AcidFolic acid 1 mg/1TabletOralBryant Ranch Prepack71335-0766
Folic AcidFolic acid 1 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-803
Folic AcidFolic acid 1 mg/1TabletOralUnit Dose Solutions, Inc.87441-032

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