What is NDC 70771-1576?

70771-1576 is the product NDC for Triazolam, Triazolam .125 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Triazolam?

13 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Triazolam NDC 70771-1576 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1576Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1576Add 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
70771-1576-1	70771157601	100 TABLET in 1 BOTTLE (70771-1576-1)Marketed from Dec 30, 2022
70771-1576-5	70771157605	500 TABLET in 1 BOTTLE (70771-1576-5)Marketed from Dec 30, 2022
70771-1576-8	70771157608	10 TABLET in 1 BOTTLE (70771-1576-8)Marketed from Dec 30, 2022

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): Triazolam
Generic name (nonproprietary): triazolam
Active ingredients: Triazolam — .125 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213003
Marketing start: Dec 30, 2022
Listing expires: Dec 31, 2026
DEA schedule: CIV
Other FDA classes: Benzodiazepines (Chemical structure)
Identifiers: Product ID 70771-1576_fb074b17-c185-44d2-9d5e-2d5836499c3aSPL ID fb074b17-c185-44d2-9d5e-2d5836499c3aSPL set ID 4084da13-5825-4399-ad69-de701508c71dRxCUI 198317, 198318UNII 1HM943223RUPC 0370710152116
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

N470771157601 followed by a unit qualifier and the quantity

Package 70771-1576-01. 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 Aug 14, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1576

What is NDC 70771-1576?: 70771-1576 is the product NDC for Triazolam, Triazolam .125 mg/1 tablet, listed with the FDA by Zydus Lifesciences Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Triazolam.
What is the active ingredient?: Triazolam.
Who is the labeler?: Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Triazolam?: 13 other product NDCs are listed under this name. See all Triazolam 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 Triazolam NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Triazolam	Triazolam .25 mg/1	TabletOral	A-S Medication Solutions	50090-7787	50090-7787-0050090-7787-01
Triazolam	Triazolam .25 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1289	70710-1289-0170710-1289-0570710-1289-08
Triazolam	Triazolam .125 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1521	70710-1521-0170710-1521-0570710-1521-08
Triazolam	Triazolam .25 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1162	70771-1162-0170771-1162-0570771-1162-08
Triazolam	Triazolam .25 mg/1	TabletOral	A-S Medication Solutions	50090-6471	50090-6471-0050090-6471-01
Triazolam	Triazolam .125 mg/1	TabletOral	Ingenus Pharmaceuticals, LLC	50742-645	50742-0645-01
Triazolam	Triazolam .25 mg/1	TabletOral	Ingenus Pharmaceuticals, LLC	50742-646	50742-0646-0150742-0646-05
Triazolam	Triazolam .25 mg/1	TabletOral	Bryant Ranch Prepack	71335-1876	71335-1876-0071335-1876-0171335-1876-02+7 more
Triazolam	Triazolam .25 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-349	72789-0349-30
Triazolam	Triazolam .25 mg/1	TabletOral	Proficient Rx LP	82804-275	82804-0275-30

All 14 Triazolam NDCs

Other NDCs under ANDA 213003

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

FDA NDC Directory listings under ANDA 213003
Product	Strength	Form · route	Labeler	Product NDC
Triazolam	Triazolam .25 mg/1	TabletOral	A-S Medication Solutions	50090-7787
Triazolam	Triazolam .25 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1289
Triazolam	Triazolam .125 mg/1	TabletOral	Zydus Pharmaceuticals USA Inc.	70710-1521
Triazolam	Triazolam .25 mg/1	TabletOral	Zydus Lifesciences Limited	70771-1162