MUPIROCIN

Product NDC
63629-9440
11-digit product format
636299440
Labeler code
63629
Product ID
63629-9440_9710426d-5e4c-41ae-96da-994f2a3025b2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
mupirocin
Dosage form
CREAM
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Application
ANDA212465
Marketing category
ANDA
Marketing start
2022-09-06
Marketing end
0000-00-00
Substance
MUPIROCIN CALCIUM
Active strength
20 mg/g
Pharmacologic classes
RNA Synthetase Inhibitor Antibacterial [EPC], RNA Synthetase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-9440-1GM - Gram63629-9440ec85aec0-5d73-489a-98bc-43894774ca3312022-10-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-9440-1636299440011 TUBE in 1 CARTON (63629-9440-1) > 30 g in 1 TUBE1 tube2022-09-150000-00-00NoNoCurrent