NDC codes

FDA NDC Directory
Product NDC (as listed)75907-224Labeler and product segments. Claims need a package NDC.
Product NDC at billing width75907-0224Add 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
75907-224-047590702240475907022404120 TABLET in 1 BOTTLE (75907-224-04)Marketed from Mar 17, 2025

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)
Abiraterone Acetate
Generic name (nonproprietary)
abiraterone acetate
Active ingredients
Abiraterone acetate — 250 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Dr. Reddys Laboratories IncNDC labeler code 75907
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208416
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 17A1 Inhibitors (Mechanism)Cytochrome P450 2C8 Inhibitors (Mechanism)Cytochrome P450 2D6 Inhibitors (Mechanism)
Identifiers
Product ID 75907-224_6c96e35d-9099-e164-0960-353b01420f81SPL ID 6c96e35d-9099-e164-0960-353b01420f81SPL set ID 0c91aa38-3b0a-232c-8eb1-55f08e8e6644RxCUI 1100075UNII EM5OCB9YJ6
Pharmacologic class
Cytochrome P450 17A1 Inhibitor

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

N475907022404 followed by a unit qualifier and the quantity

Package 75907-0224-04. 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)

Abiraterone acetate tablets are indicated in combination with prednisone for the treatment of patients with Metastatic castration-resistant prostate cancer (CRPC) Metastatic high-risk castration-sensitive prostate cancer (CSPC) Abiraterone acetate tablet is a CYP17 inhibitor indicated in combination with prednisone for the treatment of patients with metastatic castration-resistant prostate cancer (CRPC). ( 1) metastatic high-risk castration-sensitive prostate cancer (CSPC). ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 75907-224

What is NDC 75907-224?
75907-224 is the product NDC for Abiraterone Acetate, Abiraterone acetate 250 mg/1 tablet, listed with the FDA by Dr. Reddys Laboratories Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Abiraterone Acetate.
What is the active ingredient?
Abiraterone acetate.
Who is the labeler?
Dr. Reddys Laboratories Inc, NDC labeler code 75907. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Abiraterone Acetate?
28 other product NDCs are listed under this name. See all Abiraterone Acetate 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 Abiraterone Acetate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Abiraterone AcetateAbiraterone acetate 250 mg/1TabletOralAvPAK50268-03250268-0032-12
Abiraterone AcetateabirateroneAbiraterone acetate 250 mg/1TabletOralAmerican Health Packaging60687-79060687-0790-21
Abiraterone AcetateAbiraterone acetate 500 mg/1TabletOralDr. Reddys Laboratories Inc43598-46843598-0468-3843598-0468-60
Abiraterone AcetateabirateroneAbiraterone acetate 250 mg/1TabletOralAmneal Pharmaceuticals LLC60219-116560219-1165-07
Abiraterone AcetateabirateroneAbiraterone acetate 500 mg/1TabletOralAmneal Pharmaceuticals LLC60219-175460219-1754-06
Abiraterone acetateAbiraterone acetate 500 mg/1Tablet, Film coatedOralFlorida Pharmaceutical Products, LLC71921-17771921-0177-06
abiraterone acetateAbiraterone acetate 250 mg/1TabletOralFlorida Pharmaceutical Products, LLC.71921-17871921-0178-20
abiraterone acetateAbiraterone acetate 500 mg/1TabletOralGlenmark Pharmaceuticals Inc., USA68462-88268462-0882-60
abiraterone acetateAbiraterone acetate 500 mg/1TabletOralNORTHSTAR RX LLC72603-11172603-0111-01
abiraterone acetateAbiraterone acetate 250 mg/1TabletOralNORTHSTAR RX LLC72603-11072603-0110-01

All 29 Abiraterone Acetate NDCs

Other NDCs under ANDA 208416

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

FDA NDC Directory listings under ANDA 208416
ProductStrengthForm · routeLabelerProduct NDC
Abiraterone AcetateAbiraterone acetate 250 mg/1TabletOralNorthStar Rx LLC16714-963
Abiraterone AcetateAbiraterone acetate 250 mg/1TabletOralDr. Reddys Laboratories Inc43598-358
Abiraterone AcetateAbiraterone acetate 500 mg/1TabletOralDr. Reddys Laboratories Inc43598-468
Abiraterone AcetateAbiraterone acetate 250 mg/1TabletOralAvPAK50268-032

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