Home NDC 67296-1434 NDC 67296-1434 - Oxycodone Hydrochloride This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 67296-1434
Package NDCs from labels 67296-1434-7, 67296-1434-6
Manufacturer Redpharm Drug, Inc
Effective date 2024-08-07
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# NDC, Effective, Action table NDC Effective Action Document Indexing SPL Related label 67296-1434-6 2026-01-29 C162847 48780-1 49896155-a14c-586f-e063-e6dba90add90 These highlights do not include all the information needed to use OXYCODONE HYDROCHLORIDE Tablets, USP safely and effectively. See full prescribing information for Oxycodone Hydrochloride Tablets, USP. OXYCODONE HYDROCHLORIDE Tablets, USP, for oral use, CII Initial U.S. Approval: 1950 67296-1434-7 2026-01-29 C162847 48780-1 49896155-a14c-586f-e063-e6dba90add90 These highlights do not include all the information needed to use OXYCODONE HYDROCHLORIDE Tablets, USP safely and effectively. See full prescribing information for Oxycodone Hydrochloride Tablets, USP. OXYCODONE HYDROCHLORIDE Tablets, USP, for oral use, CII Initial U.S. Approval: 1950
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67296-1434-6 Oxycodone Hydrochloride 6 in 1 BOTTLE TABLET 6 2 67296-1434-7 Oxycodone Hydrochloride 12 in 1 BOTTLE, PLASTIC TABLET 12 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67296-1434 OXYCODONE HYDROCHLORIDE TABLET [REDPHARM DRUG, INC] 2 2 package rows 20240808_f45f04ea-5bb9-e8b6-e053-2a95a90a4d84.zip