Mometasone Furoate

Product NDC
0713-0726
11-digit product format
007130726
Labeler code
0713
Product ID
0713-0726_dde31996-2f38-1215-e053-2a95a90a3f54
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mometasone Furoate
Dosage form
CREAM
Route
TOPICAL
Labeler
Cosette Pharmaceuticals, Inc.
Application
ANDA077447
Marketing category
ANDA
Marketing start
2006-05-22
Marketing end
2022-08-31
Substance
MOMETASONE FUROATE
Active strength
1 mg/g
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0713-0726-15GM - Gram0713-07266f0255f9-6a57-46e5-a85c-0b3b771c4c1c12018-10-11
0713-0726-37GM - Gram0713-0726ad96ef1c-f6d8-41b3-89a1-291224e48dcf12018-10-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0713-0726-15007130726151 TUBE in 1 CARTON (0713-0726-15) > 15 g in 1 TUBE1 tube2018-08-240000-00-00NoNoCurrent
0713-0726-37007130726371 TUBE in 1 CARTON (0713-0726-37) > 45 g in 1 TUBE1 tube2018-08-240000-00-00NoNoCurrent