NDC 71335-9701 – Hydromorphone Hydrochloride

Hydromorphone Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-9701

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 (10)

Package NDCDescriptionSince
71335-9701-090 TABLET in 1 BOTTLE, PLASTIC (71335-9701-0)Feb 26, 2025
71335-9701-130 TABLET in 1 BOTTLE, PLASTIC (71335-9701-1)Jan 12, 2026
71335-9701-2180 TABLET in 1 BOTTLE, PLASTIC (71335-9701-2)Apr 10, 2026
71335-9701-3120 TABLET in 1 BOTTLE, PLASTIC (71335-9701-3)Apr 10, 2026
71335-9701-420 TABLET in 1 BOTTLE, PLASTIC (71335-9701-4)Apr 10, 2026
71335-9701-525 TABLET in 1 BOTTLE, PLASTIC (71335-9701-5)Apr 10, 2026
71335-9701-6100 TABLET in 1 BOTTLE, PLASTIC (71335-9701-6)Apr 10, 2026
71335-9701-760 TABLET in 1 BOTTLE, PLASTIC (71335-9701-7)Jul 30, 2024
71335-9701-856 TABLET in 1 BOTTLE, PLASTIC (71335-9701-8)Apr 10, 2026
71335-9701-9140 TABLET in 1 BOTTLE, PLASTIC (71335-9701-9)Apr 10, 2026

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