NDC 51672-4044 – Clorazepate Dipotassium

Clorazepate Dipotassium 15 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC51672-4044

Product details

Brand name
Clorazepate Dipotassium
Generic name
Clorazepate Dipotassium
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075731
Marketed since
April 27, 2000
Listing expires
December 31, 2027
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Clorazepate Dipotassium →

Package NDC codes (3)

Package NDCDescriptionSince
51672-4044-1100 TABLET in 1 BOTTLE (51672-4044-1)Apr 27, 2000
51672-4044-2500 TABLET in 1 BOTTLE (51672-4044-2)Apr 27, 2000
51672-4044-31000 TABLET in 1 BOTTLE (51672-4044-3)Apr 27, 2000

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