NDC 82804-065 – Glimepiride

Glimepiride 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-065

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202759
Marketed since
June 29, 2012
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (4)

Package NDCDescriptionSince
82804-065-3030 TABLET in 1 BOTTLE (82804-065-30)Jan 31, 2024
82804-065-6060 TABLET in 1 BOTTLE (82804-065-60)Jan 31, 2024
82804-065-78180 TABLET in 1 BOTTLE (82804-065-78)Feb 18, 2026
82804-065-9090 TABLET in 1 BOTTLE (82804-065-90)Jan 31, 2024

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