NDC 13107-283 – Clorazepate Dipotassium

Clorazepate Dipotassium 7.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV 2 recalls

Product NDC13107-283

Product details

Brand name
Clorazepate Dipotassium
Generic name
Clorazepate Dipotassium
Labeler
Aurolife Pharma LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071858
Marketed since
September 23, 2023
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
13107-283-01100 TABLET in 1 BOTTLE, PLASTIC (13107-283-01)Sep 23, 2023
13107-283-05500 TABLET in 1 BOTTLE, PLASTIC (13107-283-05)Sep 23, 2023

Recalls mentioning this NDC

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