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Acarbose

NDC 72789-133 · PD-Rx Pharmaceuticals, Inc.

Generic nameAcarbose
Dosage formTABLET
RouteORAL
Active ingredient(s)ACARBOSE
Strength100 mg/1
Pharmacologic classalpha Glucosidase Inhibitors [MoA], alpha-Glucosidase Inhibitor [EPC]
Marketing categoryANDA

Packages

72789-133-01 — 100 TABLET in 1 BOTTLE, PLASTIC (72789-133-01)

72789-133-30 — 30 TABLET in 1 BOTTLE, PLASTIC (72789-133-30)

72789-133-60 — 60 TABLET in 1 BOTTLE, PLASTIC (72789-133-60)

72789-133-90 — 90 TABLET in 1 BOTTLE, PLASTIC (72789-133-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0054-0140 — Acarbose, 0054-0141 — Acarbose, 0054-0142 — Acarbose, 23155-147 — Acarbose, 23155-148 — Acarbose, 23155-149 — Acarbose, 62135-453 — acarbose, 62135-454 — acarbose, 62135-455 — acarbose, 63629-5698 — acarbose, 64380-758 — acarbose, 64380-759 — acarbose, 64380-760 — acarbose, 71335-9725 — Acarbose, 72789-131 — Acarbose, 72789-132 — Acarbose

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