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Pregabalin

NDC 72888-049 · Advagen Pharma Ltd.

Generic namePregabalin
Dosage formTABLET, FILM COATED, EXTENDED RELEASE
RouteORAL
Active ingredient(s)PREGABALIN
Strength82.5 mg/1
DEA scheduleCV
Marketing categoryANDA

Packages

72888-049-30 — 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-049-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72603-357 — Pregabalin, 72603-358 — Pregabalin, 72658-0808 — PREGABALIN, 72658-0809 — PREGABALIN, 72658-0810 — PREGABALIN, 72658-0811 — PREGABALIN, 72658-0812 — PREGABALIN, 72658-0813 — PREGABALIN, 72658-0814 — PREGABALIN, 72658-0849 — PREGABALIN, 72888-050 — Pregabalin, 72888-051 — Pregabalin, 73190-053 — Pregabalin, 73190-054 — Pregabalin, 73190-055 — Pregabalin, 73190-056 — Pregabalin, 73190-057 — Pregabalin, 73190-058 — Pregabalin, 73190-059 — Pregabalin, 73190-060 — 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