Miconazole 7

Product NDC
68071-3219
11-digit product format
680713219
Labeler code
68071
Product ID
68071-3219_9a27bf4f-3c99-fb85-e053-2a95a90aafc2
Type
HUMAN OTC DRUG
Nonproprietary name
Miconazole Nitrate
Dosage form
CREAM
Route
VAGINAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA074164
Marketing category
ANDA
Marketing start
2011-09-16
Marketing end
0000-00-00
Substance
MICONAZOLE NITRATE
Active strength
20 mg/g
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-3219-72024-07-30C16284748780-1ba0f9c33-4014-a910-e053-dadaa90a0b8555270c7a-72d8-644d-e054-00144ff8d46c
68071-3219-72021-01-29C16284748780-1ba0f9c33-4014-a910-e053-dadaa90a0b8555270c7a-72d8-644d-e054-00144ff8d46c