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Oxycodone Hydrochloride

NDC 71930-023 · Eywa Pharma Inc

Generic nameOxycodone hydrochloride
Dosage formSOLUTION
RouteORAL
Active ingredient(s)OXYCODONE HYDROCHLORIDE
Strength20 mg/mL
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

71930-023-30 — 1 BOTTLE in 1 CARTON (71930-023-30) / 30 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-1959 — Oxycodone and Acetaminophen, 71335-2041 — Oxycodone and Acetaminophen, 71335-2049 — oxycodone and acetaminophen, 71335-2106 — Oxycodone and Acetaminophen, 71335-2126 — Oxycodone Hydrochloride, 71335-2182 — Oxycodone and Acetaminophen, 71335-2816 — Oxycodone Hydrochloride, 71335-9674 — oxycodone and acetaminophen, 71335-9675 — oxycodone and acetaminophen, 71930-022 — Oxycodone Hydrochloride, 71930-045 — oxycodone and acetaminophen, 71930-046 — oxycodone and acetaminophen, 71930-047 — oxycodone and acetaminophen, 72162-1334 — Oxycodone Hydrochloride, 72162-1335 — Oxycodone Hydrochloride, 72162-1336 — Oxycodone Hydrochloride, 72162-1337 — Oxycodone Hydrochloride, 72162-1338 — Oxycodone and Acetaminophen, 72162-1339 — Oxycodone and Acetaminophen, 72162-1728 — Oxycodone and Acetaminophen, +267 more

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