NDC 63629-4284 – Hydromorphone Hydrochloride

Hydromorphone Hydrochloride 2 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC63629-4284

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA019892
Marketed since
November 23, 2009
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
63629-4284-125 TABLET in 1 BOTTLE (63629-4284-1)Jun 21, 2010
63629-4284-260 TABLET in 1 BOTTLE (63629-4284-2)Aug 23, 2011
63629-4284-330 TABLET in 1 BOTTLE (63629-4284-3)Oct 22, 2010
63629-4284-428 TABLET in 1 BOTTLE (63629-4284-4)Nov 12, 2010
63629-4284-590 TABLET in 1 BOTTLE (63629-4284-5)Jun 11, 2014
63629-4284-6120 TABLET in 1 BOTTLE (63629-4284-6)Jun 25, 2012
63629-4284-740 TABLET in 1 BOTTLE (63629-4284-7)Jan 27, 2014
63629-4284-820 TABLET in 1 BOTTLE (63629-4284-8)May 1, 2012
63629-4284-910 TABLET in 1 BOTTLE (63629-4284-9)Aug 24, 2020

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