NDC 13811-702 – Hydromorphone Hydrochloride

Hydromorphone Hydrochloride 12 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC13811-702

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
Trigen Laboratories, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA205629
Marketed since
September 15, 2016
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
13811-702-10100 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-702-10)Sep 15, 2016

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