NDC 71335-2239 – Diazepam

Diazepam 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-2239

Product details

Brand name
Diazepam
Generic name
Diazepam
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA070325
Marketed since
September 4, 1985
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Diazepam →

Package NDC codes (10)

Package NDCDescriptionSince
71335-2239-0120 TABLET in 1 BOTTLE, PLASTIC (71335-2239-0)Sep 22, 2023
71335-2239-112 TABLET in 1 BOTTLE, PLASTIC (71335-2239-1)Sep 22, 2023
71335-2239-215 TABLET in 1 BOTTLE, PLASTIC (71335-2239-2)Sep 22, 2023
71335-2239-320 TABLET in 1 BOTTLE, PLASTIC (71335-2239-3)Sep 22, 2023
71335-2239-430 TABLET in 1 BOTTLE, PLASTIC (71335-2239-4)Sep 22, 2023
71335-2239-560 TABLET in 1 BOTTLE, PLASTIC (71335-2239-5)Sep 22, 2023
71335-2239-690 TABLET in 1 BOTTLE, PLASTIC (71335-2239-6)Sep 22, 2023
71335-2239-710 TABLET in 1 BOTTLE, PLASTIC (71335-2239-7)Sep 22, 2023
71335-2239-82 TABLET in 1 BOTTLE, PLASTIC (71335-2239-8)Sep 22, 2023
71335-2239-91 TABLET in 1 BOTTLE, PLASTIC (71335-2239-9)Sep 22, 2023

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