Home NDC 69364-3143 Naltrexone
Product NDC 69364-3143
11-digit product format 693643143
Labeler code 69364
Product ID 69364-3143_7b0350b5-ca48-4aef-8b10-ebd9f51967d0
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name naltrexone
Dosage form IMPLANT
Route SUBCUTANEOUS
Labeler Complete Pharmacy and Medical Solutions
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2018-02-01
Marketing end 0000-00-00
Substance NALTREXONE; TRIAMCINOLONE
Active strength 200 mg/1; mg/1
Pharmacologic classes Opioid Antagonist [EPC],Opioid Antagonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag No
Listing certified through 2019-12-31
Current FDA listing Historical FDA.report record DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69364-3143-6 Naltrexone 6 in 1 BOX IMPLANT 6 1 69364-3143-6 Naltrexone 1 in 1 BLISTER PACK IMPLANT 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69364-3143 NALTREXONE IMPLANT [COMPLETE PHARMACY AND MEDICAL SOLUTIONS] 1 Legacy NDC, 2 package rows 20180424_40b16844-bc1c-485e-aad3-2cb86e2eb009.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 69364-3143-6 69364314306 6 in 1 BOX Historical