Metronidazole

Product NDC
68788-7557
11-digit product format
687887557
Labeler code
68788
Product ID
68788-7557_d9f87ba1-5c10-41d5-bf05-3357dcfaf772
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metronidazole
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA079067
Marketing category
ANDA
Marketing start
2016-12-01
Marketing end
0000-00-00
Substance
METRONIDAZOLE
Active strength
500 mg/1
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7557-16878875570114 TABLET in 1 BOTTLE (68788-7557-1) 14 tablet2019-12-270000-00-00NoNoCurrent
68788-7557-26878875570221 TABLET in 1 BOTTLE (68788-7557-2) 21 tablet2019-12-270000-00-00NoNoCurrent
68788-7557-36878875570330 TABLET in 1 BOTTLE (68788-7557-3) 30 tablet2019-12-270000-00-00NoNoCurrent
68788-7557-46878875570428 TABLET in 1 BOTTLE (68788-7557-4) 28 tablet2019-12-270000-00-00NoNoCurrent
68788-7557-56878875570556 TABLET in 1 BOTTLE (68788-7557-5) 56 tablet2019-12-270000-00-00NoNoCurrent
68788-7557-76878875570742 TABLET in 1 BOTTLE (68788-7557-7) 42 tablet2019-12-270000-00-00NoNoCurrent