NDC 65862-580 – Glimepiride

Glimepiride 2 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC65862-580

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Aurobindo Pharma Limited
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 (3)

Package NDCDescriptionSince
65862-580-01100 TABLET in 1 BOTTLE (65862-580-01)Jun 29, 2012
65862-580-05500 TABLET in 1 BOTTLE (65862-580-05)Jun 29, 2012
65862-580-991000 TABLET in 1 BOTTLE (65862-580-99)Jun 29, 2012

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