NDC 13107-107 – Hydromorphone Hydrochloride

Hydromorphone Hydrochloride 2 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC13107-107

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
Aurolife Pharma, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205814
Marketed since
May 17, 2016
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
13107-107-01100 TABLET in 1 BOTTLE (13107-107-01)May 17, 2016
13107-107-05500 TABLET in 1 BOTTLE (13107-107-05)May 17, 2016
13107-107-2020 TABLET in 1 BOTTLE (13107-107-20)May 17, 2016
13107-107-991000 TABLET in 1 BOTTLE (13107-107-99)May 17, 2016

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