Oxycodone Hydrochloride

Product NDC: 66689-025
11-digit product format: 666890025
Labeler code: 66689
Product ID: 66689-025_505b4182-e9b4-42de-8d24-df2389aa966c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Oxycodone Hydrochloride
Dosage form: SOLUTION
Route: ORAL
Labeler: VistaPharm, Inc.
Application: ANDA202537
Marketing category: ANDA
Marketing start: 2012-08-15
Marketing end: 0000-00-00
Substance: OXYCODONE HYDROCHLORIDE
Active strength: 100 mg/5mL
Pharmacologic classes: Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule: CII
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
66689-025-30	2024-01-30	C162847	48780-1	1030e365-05b0-111a-e063-dadaa90a10e2	7c686a46-1f5f-46e3-945b-2ade3931718f

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
66689-025-30	ML - Milliliter	66689-025	ba0b8fb0-43d1-4a08-b873-aeec479e19f1	1	2013-02-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
66689-025-30	66689002530	30 mL in 1 BOTTLE (66689-025-30)	30 ml	2012-08-15	0000-00-00	No	No	Current