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Hydromorphone Hydrochloride

NDC 0641-2341 · Hikma Pharmaceuticals USA Inc.

Generic nameHydromorphone Hydrochloride
Dosage formINJECTION
RouteINTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Active ingredient(s)HYDROMORPHONE HYDROCHLORIDE
Strength2 mg/mL
Pharmacologic classFull Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA scheduleCII
Marketing categoryUNAPPROVED DRUG OTHER

Packages

0641-2341-41 — 20 VIAL in 1 CARTON (0641-2341-41) / 20 mL in 1 VIAL (0641-2341-39)

Billed under HCPCS

J1171 — Injection, hydromorphone, 0.1 mg Medicare Part B payment limit (ASP + 6%): $0.14

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0409-1312 — HYDROMORPHONE HYDROCHLORIDE, 0409-1805 — HYDROMORPHONE HYDROCHLORIDE, 0409-2634 — Hydromorphone Hydrochloride, 0409-3365 — HYDROMORPHONE HYDROCHLORIDE, 0409-4264 — HYDROMORPHONE HYDROCHLORIDE, 0574-0293 — hydromorphone hydrochloride, 0574-0294 — hydromorphone hydrochloride, 0574-0295 — hydromorphone hydrochloride, 0574-0297 — hydromorphone hydrochloride, 0574-7224 — HYDROMORPHONE HYDROCHLORIDE, 0641-6151 — Hydromorphone Hydrochloride, 0641-6169 — Hydromorphone Hydrochloride, 0641-6170 — Hydromorphone Hydrochloride, 0641-6206 — Hydromorphone Hydrochloride, 0641-6254 — Hydromorphone Hydrochloride, 0641-6259 — Hydromorphone Hydrochloride, 0703-0018 — HYDROMORPHONE HYDROCHLORIDE, 0703-0110 — HYDROMORPHONE HYDROCHLORIDE, 0703-0113 — HYDROMORPHONE HYDROCHLORIDE, 13107-107 — 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.