Oxycodone Hydrochloride 67296-2188-01

Package NDC

67296-2188-01

Product NDC: 67296-2188

Manufacturer: Redpharm Drug
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
DEA Schedule: Schedule CII
Marketing Start: September 10, 2024
Listing Expires: December 31, 2026
Application: ANDA077712

Active Ingredients

Ingredient	Strength
Oxycodone Hydrochloride	5 mg/1

Drug Class

Full Opioid Agonists [MoA]Opioid Agonist [EPC]

Selected Package

67296-2188-01Selected

12 TABLET in 1 BOTTLE, PLASTIC (67296-2188-1)

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External Resources

FDA Drug Database DailyMed Label