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Alendronate Sodium

NDC 0054-0282 · Hikma Pharmaceuticals USA Inc.

Generic nameAlendronate Sodium
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ALENDRONATE SODIUM
Strength70 mg/75mL
Pharmacologic classBisphosphonate [EPC], Diphosphonates [CS]
Marketing categoryANDA

Packages

0054-0282-59 — 4 BOTTLE, UNIT-DOSE in 1 CARTON (0054-0282-59) / 75 mL in 1 BOTTLE, UNIT-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0115-1676 — Alendronate Sodium, 0115-1678 — Alendronate Sodium, 0115-1679 — Alendronate Sodium, 0115-1680 — Alendronate Sodium, 0115-1681 — Alendronate Sodium, 10135-718 — Alendronate sodium tablet, 10135-719 — Alendronate sodium tablet, 16714-631 — Alendronate Sodium, 16714-632 — Alendronate Sodium, 16714-633 — Alendronate Sodium, 50090-3126 — Alendronate Sodium, 50090-4692 — Alendronate sodium, 50090-5474 — Alendronate Sodium, 50090-5677 — Alendronate Sodium, 60723-205 — ALENDRONATE SODIUM, 60723-207 — ALENDRONATE SODIUM, 64980-340 — Alendronate Sodium, 64980-341 — Alendronate Sodium, 64980-342 — Alendronate Sodium, 65862-327 — Alendronate Sodium, +17 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