NDC 60687-579 – Hydromorphone Hydrochloride

Hydromorphone Hydrochloride 2 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC60687-579

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076855
Marketed since
May 11, 2021
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
60687-579-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-579-01) / 1 TABLET in 1 BLISTER PACK (60687-579-11)May 11, 2021

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