NDC 71335-1876 – Triazolam

Triazolam .25 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1876

Product details

Brand name
Triazolam
Generic name
Triazolam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214219
Marketed since
October 20, 2020
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Triazolam →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1876-03 TABLET in 1 BOTTLE, PLASTIC (71335-1876-0)Dec 29, 2021
71335-1876-110 TABLET in 1 BOTTLE, PLASTIC (71335-1876-1)Dec 29, 2021
71335-1876-230 TABLET in 1 BOTTLE, PLASTIC (71335-1876-2)Jun 8, 2021
71335-1876-360 TABLET in 1 BOTTLE, PLASTIC (71335-1876-3)Dec 29, 2021
71335-1876-440 TABLET in 1 BOTTLE, PLASTIC (71335-1876-4)Dec 29, 2021
71335-1876-590 TABLET in 1 BOTTLE, PLASTIC (71335-1876-5)Dec 29, 2021
71335-1876-66 TABLET in 1 BOTTLE, PLASTIC (71335-1876-6)Dec 29, 2021
71335-1876-71 TABLET in 1 BOTTLE, PLASTIC (71335-1876-7)Dec 3, 2021
71335-1876-82 TABLET in 1 BOTTLE, PLASTIC (71335-1876-8)Sep 7, 2021
71335-1876-928 TABLET in 1 BOTTLE, PLASTIC (71335-1876-9)Dec 29, 2021

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