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ALENDRONATE SODIUM

NDC 68071-3340 · NuCare Pharmaceuticals,Inc.

Generic nameAlendronate sodium
Dosage formTABLET
RouteORAL
Active ingredient(s)ALENDRONATE SODIUM
Strength70 mg/1
Pharmacologic classBisphosphonate [EPC], Diphosphonates [CS]
Marketing categoryANDA

Packages

68071-3340-4 — 4 TABLET in 1 BOX (68071-3340-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 65862-328 — Alendronate Sodium, 65862-329 — Alendronate Sodium, 68071-3771 — Alendronate sodium, 68788-7130 — Alendronate sodium, 69097-223 — Alendronate sodium, 69097-224 — Alendronate sodium, 70518-0033 — Alendronate sodium, 70518-1192 — Alendronate sodium, 70539-400 — alendronate sodium, 70954-264 — Alendronate Sodium, 71205-048 — Alendronate Sodium, 76282-681 — 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