NDC codes

FDA NDC Directory
Product NDC (as listed)80725-005Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80725-0005Add 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
80725-005-018072500050180725000501100 TABLET in 1 BOTTLE (80725-005-01)Marketed from Apr 4, 2022

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)
Valium
Generic name (nonproprietary)
diazepam
Active ingredients
Diazepam — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Waylis Therapeutics LLCNDC labeler code 80725
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 013263
Marketing start
Listing expires
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 80725-005_a17d4f0b-e415-4921-b0f9-9e7a1b6e1db5SPL ID a17d4f0b-e415-4921-b0f9-9e7a1b6e1db5
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

N480725000501 followed by a unit qualifier and the quantity

Package 80725-0005-01. 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

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

About NDC 80725-005

What is NDC 80725-005?
80725-005 is the product NDC for Valium (diazepam), Diazepam 5 mg/1 tablet, listed with the FDA by Waylis Therapeutics LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Valium (Diazepam).
What is the active ingredient?
Diazepam.
Who is the labeler?
Waylis Therapeutics LLC, NDC labeler code 80725. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Valium?
4 other product NDCs are listed under this name. See all Valium 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 Valium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ValiumdiazepamDiazepam 2 mg/1TabletOralWaylis Therapeutics LLC80725-00480725-0004-01
ValiumdiazepamDiazepam 10 mg/1TabletOralWaylis Therapeutics LLC80725-00680725-0006-01
ValiumdiazepamDiazepam 2 mg/1TabletOralRoche Laboratories Inc.0140-000400140-0004-01
ValiumdiazepamDiazepam 5 mg/1TabletOralRoche Laboratories Inc.0140-000500140-0005-0100140-0005-14

Other NDCs under NDA 013263

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

FDA NDC Directory listings under NDA 013263
ProductStrengthForm · routeLabelerProduct NDC
ValiumdiazepamDiazepam 2 mg/1TabletOralRoche Laboratories Inc.0140-0004
ValiumdiazepamDiazepam 5 mg/1TabletOralRoche Laboratories Inc.0140-0005
ValiumdiazepamDiazepam 2 mg/1TabletOralWaylis Therapeutics LLC80725-004
ValiumdiazepamDiazepam 10 mg/1TabletOralWaylis Therapeutics LLC80725-006

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