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Glimepiride

NDC 43063-699 · PD-Rx Pharmaceuticals, Inc.

Generic nameGlimepiride

Dosage formTABLET

RouteORAL

Active ingredient(s)GLIMEPIRIDE

Strength4 mg/1

Pharmacologic classSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Marketing categoryANDA

Packages

43063-699-90 — 90 TABLET in 1 BOTTLE, PLASTIC (43063-699-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 43063-946 — Glimepiride, 43547-394 — glimepiride, 43547-395 — glimepiride, 43547-396 — glimepiride, 50090-1006 — Glimepiride, 50090-6322 — Glimepiride, 50090-6394 — Glimepiride, 50090-6415 — Glimepiride, 50090-6426 — Glimepiride, 50090-6852 — 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