NDC 70710-1521 – Triazolam

Triazolam .125 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC70710-1521

Product details

Brand name
Triazolam
Generic name
Triazolam
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213003
Marketed since
December 30, 2022
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Triazolam →

Package NDC codes (3)

Package NDCDescriptionSince
70710-1521-1100 TABLET in 1 BOTTLE (70710-1521-1)Dec 30, 2022
70710-1521-5500 TABLET in 1 BOTTLE (70710-1521-5)Dec 30, 2022
70710-1521-810 TABLET in 1 BOTTLE (70710-1521-8)Dec 30, 2022

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