NDC 72865-171 – Hydromorphone hydrochloride

Hydromorphone Hydrochloride 32 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC72865-171

Product details

Brand name
Hydromorphone hydrochloride
Generic name
Hydromorphone hydrochloride
Labeler
XLCare Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212133
Marketed since
September 24, 2020
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Hydromorphone Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
72865-171-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-171-01)Sep 24, 2020

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