NDC 68682-655 – Diazepam

Diazepam 20 mg/4mL · Gel · Rectal

Human Prescription Drug DEA schedule CIV 1 recall

Product NDC68682-655

Product details

Brand name
Diazepam
Generic name
Diazepam
Labeler
Oceanside Pharmaceuticals
Dosage form
Gel
Route
Rectal
Marketing category
NDA AUTHORIZED GENERIC · NDA020648
Marketed since
July 29, 1997
Listing expires
December 31, 2026
Pharmacologic class
Benzodiazepine

Active ingredients

Uses, dosage, side effects and warnings for Diazepam →

Package NDC codes (1)

Package NDCDescriptionSince
68682-655-202 SYRINGE, PLASTIC in 1 PACKAGE (68682-655-20) / 4 mL in 1 SYRINGE, PLASTICJul 29, 1997

Recalls mentioning this NDC

Other Diazepam products