Mondoxyne NL

Product NDC
69668-452
11-digit product format
696680452
Labeler code
69668
Product ID
69668-452_95999290-0a2d-70e8-e053-2a95a90a8df5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Doxycycline
Dosage form
CAPSULE
Route
ORAL
Labeler
Sonoma Pharmaceuticals, Inc.
Application
ANDA204446
Marketing category
ANDA
Marketing start
2015-05-28
Marketing end
0000-00-00
Substance
DOXYCYCLINE
Active strength
75 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC],Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69668-452-01EA - Each69668-452a488ac10-64a1-4de2-9cd2-337c8f3ad47712018-11-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69668-452-016966804520160 CAPSULE in 1 BOTTLE, PLASTIC (69668-452-01) 60 capsule2018-10-040000-00-00NoNoCurrent
69668-452-04696680452042 CAPSULE in 1 BOTTLE, PLASTIC (69668-452-04) 2 capsule2018-11-140000-00-00YesNoCurrent