NDC codes

FDA NDC Directory
Product NDC (as listed)80425-0120Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80425-0120Add 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
80425-0120-28042501200260 TABLET in 1 BOTTLE (80425-0120-2)Marketed from Dec 10, 1986

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Diazepam
Generic name (nonproprietary)
diazepam
Active ingredients
Diazepam — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 071322
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 80425-0120_2a999573-1032-813a-e063-6294a90a49b1SPL ID 2a999573-1032-813a-e063-6294a90a49b1SPL set ID b7002d26-3856-4c2f-e053-2995a90aea60RxCUI 197589UNII Q3JTX2Q7TU
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

N480425012002 followed by a unit qualifier and the quantity

Package 80425-0120-02. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 071322

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

FDA NDC Directory listings under ANDA 071322
ProductStrengthForm · routeLabelerProduct NDC
DiazepamDiazepam 10 mg/1TabletOralREMEDYREPACK INC.70518-0162
DiazepamDiazepam 10 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-424
DiazepamDiazepam 10 mg/1TabletOralA-S Medication Solutions50090-1726
DiazepamDiazepam 10 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0172-3927
DiazepamDiazepam 10 mg/1TabletOralBryant Ranch Prepack71335-0444
DiazepamDiazepam 10 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-987
DiazepamDiazepam 10 mg/1TabletOralAsclemed USA, Inc.76420-784
DiazepamDiazepam 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4829
DiazepamDiazepam 10 mg/1TabletOralDirect_Rx61919-906
DiazepamDiazepam 10 mg/1TabletOralCoupler LLC67046-0944
DiazepamDiazepam 10 mg/1TabletOralREMEDYREPACK INC.70518-0014
DiazepamDiazepam 10 mg/1TabletOralProficient Rx LP63187-544

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