NDC codes

FDA NDC Directory
Product NDC (as listed)50268-032Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50268-0032Add 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
50268-032-125026800321220 BLISTER PACK in 1 BOX (50268-032-12) / 1 TABLET in 1 BLISTER PACK (50268-032-11)Marketed from May 4, 2026

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
AvPAK
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 50268-032_5108abe6-98f5-ce57-e063-6394a90aef2fSPL ID 5108abe6-98f5-ce57-e063-6394a90aef2fSPL set ID 5108c2fe-9706-c976-e063-6294a90a796dRxCUI 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

N450268003212 followed by a unit qualifier and the quantity

Package 50268-0032-12. 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)

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/1TabletOralDr. Reddys Laboratories Inc43598-358
Abiraterone AcetateAbiraterone acetate 500 mg/1TabletOralDr. Reddys Laboratories Inc43598-468
Abiraterone AcetateAbiraterone acetate 250 mg/1TabletOralNorthStar Rx LLC16714-963
Abiraterone AcetateAbiraterone acetate 250 mg/1TabletOralDr. Reddys Laboratories Inc75907-224

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