NDC 70518-4137 – Alprazolam

Alprazolam 1 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC70518-4137

Product details

Brand name
Alprazolam
Generic name
Alprazolam
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074112
Marketed since
July 10, 2024
Marketing end
March 19, 2027
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Alprazolam →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4137-060 TABLET in 1 BOTTLE, PLASTIC (70518-4137-0)Jul 10, 2024

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