Oxazepam NDC 0228-2069

Unfinished product

This listing is a drug for further processing, not a finished drug product dispensed or administered to patients. It is not normally billed.

NDC codes

FDA NDC Directory

Product NDC (as listed)0228-2069Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00228-2069Add 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	Copy
0228-2069-00	00228206900	12020 CAPSULE, GELATIN COATED in 1 BOX (0228-2069-00)Marketed from 29-SEP-23
0228-2069-77	00228206977	12020 CAPSULE, GELATIN COATED in 1 CONTAINER (0228-2069-77)Marketed from 20-MAR-25

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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

Generic name (nonproprietary): oxazepam
Active ingredients: Oxazepam — 15 mg/1
Dosage form: Capsule, Gelatin coated
Labeler: Actavis Pharma, Inc.
Product type: Drug for further processing
Marketing category: Drug for further processing
Marketing start: Sep 29, 2023
Listing expires: Dec 31, 2026
DEA schedule: CIV
Identifiers: Product ID 0228-2069_e7e7c971-1a52-4417-bbd0-94fbdf491631SPL ID e7e7c971-1a52-4417-bbd0-94fbdf491631

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N400228206900 followed by a unit qualifier and the quantity

Package 00228-2069-00. 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

The FDA listing for this product does not reference a label (SPL) set.