NDC 71335-1584 – Diazepam

Diazepam 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1584

Product details

Brand name
Diazepam
Generic name
Diazepam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071321
Marketed since
December 10, 1986
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Diazepam →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1584-0120 TABLET in 1 BOTTLE (71335-1584-0)Feb 10, 2022
71335-1584-112 TABLET in 1 BOTTLE (71335-1584-1)Feb 10, 2022
71335-1584-215 TABLET in 1 BOTTLE (71335-1584-2)Feb 10, 2022
71335-1584-320 TABLET in 1 BOTTLE (71335-1584-3)Feb 10, 2022
71335-1584-430 TABLET in 1 BOTTLE (71335-1584-4)Feb 10, 2022
71335-1584-560 TABLET in 1 BOTTLE (71335-1584-5)Feb 10, 2022
71335-1584-690 TABLET in 1 BOTTLE (71335-1584-6)Feb 10, 2022
71335-1584-710 TABLET in 1 BOTTLE (71335-1584-7)Feb 10, 2022
71335-1584-82 TABLET in 1 BOTTLE (71335-1584-8)Feb 10, 2022
71335-1584-91 TABLET in 1 BOTTLE (71335-1584-9)Feb 10, 2022

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