NDC 0781-1061 – Alprazolam

Alprazolam .25 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC0781-1061

Product details

Brand name
Alprazolam
Generic name
Alprazolam
Labeler
Sandoz Inc
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074112
Marketed since
December 29, 1995
Marketing end
March 19, 2027
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Alprazolam →

Package NDC codes (3)

Package NDCDescriptionSince
0781-1061-01100 TABLET in 1 BOTTLE (0781-1061-01)Dec 29, 1995
0781-1061-05500 TABLET in 1 BOTTLE (0781-1061-05)Dec 29, 1995
0781-1061-101000 TABLET in 1 BOTTLE (0781-1061-10)Dec 29, 1995

Recalls mentioning this NDC

Other Alprazolam products