Miconazole 7

Product NDC
68071-1703
11-digit product format
680711703
Labeler code
68071
Product ID
68071-1703_d6ac754b-27df-2937-e053-2995a90a2954
Type
HUMAN OTC DRUG
Nonproprietary name
Miconazole Nitrate
Dosage form
CREAM
Route
VAGINAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA074164
Marketing category
ANDA
Marketing start
1997-04-01
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-1703-72022-05-31C16284748780-1d6a99b39-d43d-a426-e053-dadaa90af4c28349d8f8-d210-377a-e053-2a91aa0a0233
68071-1703-72022-01-28C16284748780-1d6a99b39-d43d-a426-e053-dadaa90af4c28349d8f8-d210-377a-e053-2a91aa0a0233

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68071-1703-7GM - Gram68071-1703776e01f4-e143-4648-96ec-3fbde2ef4abc12019-03-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68071-1703-76807117030745 g in 1 BOX (68071-1703-7) 45 g2019-03-040000-00-00NoNoCurrent