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PREGABALIN

NDC 82619-122 · Creekwood Pharmaceuticals LLC

Generic namePregabalin
Dosage formCAPSULE
RouteORAL
Active ingredient(s)PREGABALIN
Strength25 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

82619-122-01 — 90 CAPSULE in 1 BOTTLE (82619-122-01)

82619-122-02 — 500 CAPSULE in 1 BOTTLE (82619-122-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

80425-0178 — Pregabalin, 80425-0185 — PREGABALIN, 80425-0277 — Pregabalin, 80425-0308 — Pregabalin, 80425-0327 — Pregabalin, 80425-0397 — PREGABALIN, 80425-0399 — PREGABALIN, 80425-0417 — PREGABALIN, 80425-0421 — PREGABALIN, 80425-0433 — Pregabalin, 82619-123 — Pregabalin, 82619-124 — Pregabalin, 82619-125 — Pregabalin, 82619-126 — Pregabalin, 82619-127 — Pregabalin, 82619-128 — Pregabalin, 82619-129 — Pregabalin, 82804-049 — PREGABALIN, 82804-170 — Pregabalin, 82804-184 — Pregabalin, +519 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