Miconazole 7

Product NDC
68016-073
11-digit product format
680160073
Labeler code
68016
Product ID
68016-073_40fa7a7f-aec8-4b4d-bcbf-2f1ea7e935f0
Type
HUMAN OTC DRUG
Nonproprietary name
Miconazole Nitrate
Dosage form
CREAM
Route
VAGINAL
Labeler
Chain Drug Consortium, LLC
Application
ANDA074164
Marketing category
ANDA
Marketing start
2003-09-11
Marketing end
0000-00-00
Substance
MICONAZOLE NITRATE
Active strength
20 mg/g
Pharmacologic classes
Azole Antifungal [EPC], Azoles [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68016-073-01GM - Gram68016-0737c926793-655e-40ac-bd1a-a1ad42f277f812014-11-05

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68016-073MICONAZOLE 7 (MICONAZOLE NITRATE) CREAM [CHAIN DRUG CONSORTIUM, LLC]11Legacy NDC20221122_74369ba9-2021-467e-bf1d-c4e7284535da.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68016-073-01680160073011 TUBE, WITH APPLICATOR in 1 CARTON (68016-073-01) > 45 g in 1 TUBE, WITH APPLICATOR2003-09-110000-00-00NoNoCurrent