NDC codes

FDA NDC Directory
Product NDC (as listed)0378-0345Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00378-0345Add 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
0378-0345-0100378034501100 TABLET in 1 BOTTLE, PLASTIC (0378-0345-01)Marketed from Sep 4, 1985
0378-0345-0500378034505500 TABLET in 1 BOTTLE, PLASTIC (0378-0345-05)Marketed from Sep 4, 1985

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

Brand name (proprietary)
Diazepam
Generic name (nonproprietary)
diazepam
Active ingredients
Diazepam — 5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070325
Marketing start
Marketing end
DEA schedule
CIV
Other FDA classes
Benzodiazepines (Chemical structure)
Identifiers
Product ID 0378-0345_038a1547-a013-48d8-b7df-2a3041882d63SPL ID 038a1547-a013-48d8-b7df-2a3041882d63
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

N400378034501 followed by a unit qualifier and the quantity

Package 00378-0345-01. 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.

Other NDCs under ANDA 070325

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

FDA NDC Directory listings under ANDA 070325
ProductStrengthForm · routeLabelerProduct NDC
DiazepamDiazepam 5 mg/1TabletOralBryant Ranch Prepack71335-2239
DiazepamDiazepam 5 mg/1TabletOralSafecor Health, LLC48433-028
DiazepamDiazepam 2 mg/1TabletOralSafecor Health, LLC48433-027
DiazepamDiazepam 10 mg/1TabletOralSafecor Health, LLC48433-029
DiazepamDiazepam 2 mg/1TabletOralBryant Ranch Prepack71335-2247
DiazepamDiazepam 10 mg/1TabletOralDirect_Rx72189-552
DiazepamDiazepam 5 mg/1TabletOralCardinal Health 107, LLC55154-5554
DiazepamDiazepam 10 mg/1TabletOralClinical Solutions Wholesale, LLC58118-4047
DiazepamDiazepam 2 mg/1TabletOralDirect_rx72189-570
DiazepamDiazepam 10 mg/1TabletOralBryant Ranch Prepack71335-2306
DiazepamDiazepam 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8462
DiazepamDiazepam 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8466
DiazepamDiazepam 10 mg/1TabletOralUnit Dose Solutions, Inc.87441-025
DiazepamDiazepam 5 mg/1TabletOralUnit Dose Solutions, Inc.87441-026
DiazepamDiazepam 10 mg/1TabletOralMylan Institutional Inc.51079-286
DiazepamDiazepam 2 mg/1TabletOralMylan Institutional Inc.51079-284
DiazepamDiazepam 5 mg/1TabletOralMylan Institutional Inc.51079-285
DiazepamDiazepam 5 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0496
DiazepamDiazepam 10 mg/1TabletOralMylan Pharmaceuticals Inc.0378-0477
DiazepamDiazepam 10 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0512

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