Metronidazole

Product NDC
0713-0757
11-digit product format
007130757
Labeler code
0713
Product ID
0713-0757_dde311f0-0ed9-e416-e053-2a95a90a860b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metronidazole
Dosage form
CREAM
Route
TOPICAL
Labeler
Cosette Pharmaceuticals, Inc.
Application
ANDA077549
Marketing category
ANDA
Marketing start
2019-05-21
Marketing end
2022-09-30
Substance
METRONIDAZOLE
Active strength
8 mg/g
Pharmacologic classes
Nitroimidazole Antimicrobial [EPC], Nitroimidazoles [CS]
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
0713-0757-37GM - Gram0713-07578da709ec-91c6-4d6a-bc5e-bb617d4864bc12019-08-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0713-0757-37007130757371 TUBE in 1 CARTON (0713-0757-37) > 45 g in 1 TUBE1 tube2019-05-210000-00-00NoNoCurrent