Mometasone Furoate

Product NDC
0713-0727
11-digit product format
007130727
Labeler code
0713
Product ID
0713-0727_dde311f0-0ef2-e416-e053-2a95a90a860b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mometasone Furoate
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Cosette Pharmaceuticals, Inc.
Application
ANDA077401
Marketing category
ANDA
Marketing start
2006-06-20
Marketing end
2022-12-31
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
0713-0727-15GM - Gram0713-072742f82329-2fb2-4bd2-939d-d495154d3d0f12018-10-11
0713-0727-37GM - Gram0713-07278ca1bbdf-b6ae-4fe2-a3e2-7978756aa6db12018-10-11

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0713-0727-15007130727151 TUBE in 1 CARTON (0713-0727-15) > 15 g in 1 TUBE1 tube2018-09-070000-00-00NoNoCurrent
0713-0727-37007130727371 TUBE in 1 CARTON (0713-0727-37) > 45 g in 1 TUBE1 tube2018-09-070000-00-00NoNoCurrent