NDC codes

FDA NDC Directory
Product NDC (as listed)62584-814Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62584-0814Add 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
62584-814-0162584081401100 BLISTER PACK in 1 CARTON (62584-814-01) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (62584-814-11)Marketed from Dec 17, 2007

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)
Oxazepam
Generic name (nonproprietary)
oxazepam
Active ingredients
Oxazepam — 30 mg/1
Dosage form
Capsule, Gelatin coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 072253
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 62584-814_26e63053-7a43-e278-e063-6394a90a23b8SPL ID 26e63053-7a43-e278-e063-6394a90a23b8SPL set ID 03440821-831c-4085-98f9-faa88e98c503RxCUI 198057, 198059, 312134UNII 6GOW6DWN2A
Pharmacologic class
Benzodiazepine

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

N462584081401 followed by a unit qualifier and the quantity

Package 62584-0814-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS Oxazepam capsules are indicated for the management of anxiety disorders or for the short-term relief of the symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. Anxiety associated with depression is also responsive to oxazepam therapy. This product has been found particularly useful in the management of anxiety, tension, agitation and irritability in older patients. Alcoholics with acute tremulousness, inebriation, or with anxiety associated with alcohol withdrawal are responsive to therapy. The effectiveness of oxazepam in long-term use, that is, more than 4 months, has not been assessed by sys…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 072253

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

FDA NDC Directory listings under ANDA 072253
ProductStrengthForm · routeLabelerProduct NDC
OxazepamOxazepam 10 mg/1Capsule, Gelatin coatedOralActavis Pharma, Inc.0228-2067
OxazepamOxazepam 15 mg/1Capsule, Gelatin coatedOralActavis Pharma, Inc.0228-2069
OxazepamOxazepam 30 mg/1Capsule, Gelatin coatedOralActavis Pharma, Inc.0228-2073
OxazepamOxazepam 10 mg/1Capsule, Gelatin coatedOralAmerican Health Packaging62584-812
OxazepamOxazepam 15 mg/1Capsule, Gelatin coatedOralAmerican Health Packaging62584-813

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Oxazepam NDC 62584-814 | Med-Code