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Glimepiride

NDC 16729-002 · Accord Healthcare Inc

Generic nameGlimepiride

Dosage formTABLET

RouteORAL

Active ingredient(s)GLIMEPIRIDE

Strength2 mg/1

Pharmacologic classSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Marketing categoryANDA

Packages

16729-002-01 — 100 TABLET in 1 BOTTLE (16729-002-01)

16729-002-16 — 500 TABLET in 1 BOTTLE (16729-002-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8332 — Glimepiride, 0615-8333 — Glimepiride, 0615-8334 — Glimepiride, 16571-773 — Glimepiride, 16571-774 — Glimepiride, 16571-775 — Glimepiride, 16729-001 — Glimepiride, 16729-003 — Glimepiride, 42571-100 — Glimepiride, 42571-101 — Glimepiride, 42571-102 — Glimepiride, 42571-103 — Glimepiride, 42571-104 — Glimepiride, 42571-105 — Glimepiride, 43063-121 — Glimepiride, 43063-122 — Glimepiride, 43063-587 — Glimepiride, 43063-630 — Glimepiride, 43063-697 — Glimepiride, 43063-698 — Glimepiride, +86 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels