Home NDC 42254-229
mupirocin
Product NDC 42254-229
11-digit product format 422540229
Labeler code 42254
Product ID 42254-229_ed49fb2a-05f6-4df5-9c75-30df41a5aae1
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Mupirocin
Dosage form OINTMENT
Route TOPICAL
Labeler Rebel Distributors Corp
Application ANDA065123
Marketing category ANDA
Marketing start 2009-10-30
Marketing end 0000-00-00
Substance MUPIROCIN
Active strength 20 mg/g
Pharmacologic classes RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]
NDC exclude flag E
Listing certified through 2017-12-31
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 42254-229-22 mupirocin 1 in 1 CARTON OINTMENT 1 1 42254-229-22 mupirocin 22 g in 1 TUBE OINTMENT 22 1
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 42254-229 MUPIROCIN OINTMENT [REBEL DISTRIBUTORS CORP] 1 Legacy NDC, 2 package rows 20130329_ed49fb2a-05f6-4df5-9c75-30df41a5aae1.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Status 42254-229-22 42254022922 1 in 1 CARTON Historical