What is NDC 71335-0444?

71335-0444 is the product NDC for Diazepam, Diazepam 10 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Diazepam?

118 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Diazepam NDC 71335-0444 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0444Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0444Add 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
71335-0444-0	71335044400	56 TABLET in 1 BOTTLE (71335-0444-0)Marketed from Apr 3, 2024
71335-0444-1	71335044401	20 TABLET in 1 BOTTLE (71335-0444-1)Marketed from Jul 26, 2019
71335-0444-2	71335044402	30 TABLET in 1 BOTTLE (71335-0444-2)Marketed from Feb 14, 2018
71335-0444-3	71335044403	40 TABLET in 1 BOTTLE (71335-0444-3)Marketed from Feb 27, 2018
71335-0444-4	71335044404	50 TABLET in 1 BOTTLE (71335-0444-4)Marketed from Apr 3, 2024
71335-0444-5	71335044405	60 TABLET in 1 BOTTLE (71335-0444-5)Marketed from Feb 19, 2018
71335-0444-6	71335044406	90 TABLET in 1 BOTTLE (71335-0444-6)Marketed from Mar 6, 2018
71335-0444-7	71335044407	100 TABLET in 1 BOTTLE (71335-0444-7)Marketed from Apr 3, 2024
71335-0444-8	71335044408	10 TABLET in 1 BOTTLE (71335-0444-8)Marketed from Mar 25, 2019
71335-0444-9	71335044409	120 TABLET in 1 BOTTLE (71335-0444-9)Marketed from Jul 23, 2018

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
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 071322
Marketing start: Dec 10, 1986
Listing expires: Dec 31, 2026
DEA schedule: CIV
Other FDA classes: Benzodiazepines (Chemical structure)
Identifiers: Product ID 71335-0444_5f5a6893-926b-4934-bdcd-b1c0efedf319SPL ID 5f5a6893-926b-4934-bdcd-b1c0efedf319SPL set ID 078bbb41-7e3a-48db-87f0-ec6a6ec0194eRxCUI 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

N471335044400 followed by a unit qualifier and the quantity

Package 71335-0444-00. 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

Current FDA label (SPL), effective Apr 3, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS Diazepam tablets 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. In acute alcohol withdrawal, diazepam tablets may be useful in the symptomatic relief of acute agitation, tremor, impending or acute delirium tremens and hallucinosis. Diazepam is a useful adjunct for the relief of skeletal muscle spasm due to reflex spasm to local pathology (such as inflammation of the muscles or joints, or secondary to trauma), spasticity caused by upper motor neuron disorders (such as cerebral palsy and paraplegia), at…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0444

What is NDC 71335-0444?: 71335-0444 is the product NDC for Diazepam, Diazepam 10 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Diazepam.
What is the active ingredient?: Diazepam.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Diazepam?: 118 other product NDCs are listed under this name. See all Diazepam 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 Diazepam NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Diazepam	Diazepam 5 mg/mL	InjectionIntramuscular, Intravenous	Civica, Inc.	72572-175	72572-0175-10
Diazepam	Diazepam 10 mg/2mL	Injection, SolutionIntramuscular, Intravenous	Baxter Healthcare Corporation	43066-121	43066-0121-10
Diazepam	Diazepam 20 mg/4mL	Injection, SolutionIntramuscular, Intravenous	Baxter Healthcare Corporation	43066-123	43066-0123-10
Diazepam	Diazepam 10 mg/2mL	Injection, SolutionIntramuscular, Intravenous	REMEDYREPACK INC.	70518-4704	70518-4704-00
Diazepam	Diazepam 5 mg/mL	Injection, SolutionIntramuscular, Intravenous	Hikma Pharmaceuticals USA Inc.	0641-6283	00641-6283-25
Diazepam	Diazepam 10 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-025	87441-0025-01
Diazepam	Diazepam 5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-026	87441-0026-01
Diazepam	Diazepam 5 mg/1	TabletOral	Coupler LLC	67046-0943	67046-0943-03
Diazepam	Diazepam 10 mg/1	TabletOral	Coupler LLC	67046-0944	67046-0944-03
Diazepam	Diazepam 5 mg/mL	InjectionIntramuscular, Intravenous	Henry Schein, Inc.	0404-9762	00404-9762-10

All 119 Diazepam NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Diazepam	Diazepam 10 mg/1	TabletOral	Proficient Rx LP	63187-544
Diazepam	Diazepam 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-0162
Diazepam	Diazepam 10 mg/1	TabletOral	Aphena Pharma Solutions - Tennessee, LLC	71610-424
Diazepam	Diazepam 10 mg/1	TabletOral	A-S Medication Solutions	50090-1726
Diazepam	Diazepam 10 mg/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0172-3927
Diazepam	Diazepam 10 mg/1	TabletOral	Asclemed USA, Inc.	76420-784
Diazepam	Diazepam 10 mg/1	TabletOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0120
Diazepam	Diazepam 10 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-987
Diazepam	Diazepam 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4829
Diazepam	Diazepam 10 mg/1	TabletOral	Coupler LLC	67046-0944
Diazepam	Diazepam 10 mg/1	TabletOral	Direct_Rx	61919-906
Diazepam	Diazepam 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-0014