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Hydromorphone Hydrochloride

NDC 13811-704 · Trigen Laboratories, LLC

Generic nameHydromorphone Hydrochloride
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)HYDROMORPHONE HYDROCHLORIDE
Strength32 mg/1
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryANDA

Packages

13811-704-10 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-704-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0641-6259 — Hydromorphone Hydrochloride, 0703-0018 — HYDROMORPHONE HYDROCHLORIDE, 0703-0110 — HYDROMORPHONE HYDROCHLORIDE, 0703-0113 — HYDROMORPHONE HYDROCHLORIDE, 13107-107 — HYDROMORPHONE HYDROCHLORIDE, 13107-108 — HYDROMORPHONE HYDROCHLORIDE, 13107-109 — HYDROMORPHONE HYDROCHLORIDE, 13811-701 — Hydromorphone Hydrochloride, 13811-702 — Hydromorphone Hydrochloride, 13811-703 — Hydromorphone Hydrochloride, 31722-119 — hydromorphone hydrochloride, 31722-120 — hydromorphone hydrochloride, 31722-121 — hydromorphone hydrochloride, 31722-122 — hydromorphone hydrochloride, 42858-122 — hydromorphone hydrochloride, 42858-234 — hydromorphone hydrochloride, 42858-301 — Hydromorphone Hydrochloride, 42858-302 — Hydromorphone Hydrochloride, 42858-303 — Hydromorphone Hydrochloride, 42858-304 — Hydromorphone Hydrochloride, +50 more

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