FDA.reportPublic FDA data

PedizolPAK

Product NDC
70859-053
11-digit product format
708590053
Labeler code
70859
Product ID
70859-053_c831548d-64db-7872-e053-2995a90a8dab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ketoconazole,Miconazole Nitrate
Dosage form
KIT
Labeler
NuCare Pharmaceuticals,Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2002-12-18
Marketing end
0000-00-00
Active strength
0
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70859-053-012024-08-12C16284748780-1ba0f9c33-28ff-a910-e053-dadaa90a0b859367e7df-b40a-4968-e053-2995a90ae8ac
70859-053-012023-01-30C16284748780-1ba0f9c33-28ff-a910-e053-dadaa90a0b859367e7df-b40a-4968-e053-2995a90ae8ac
70859-053-012021-05-04C16284748780-1ba0f9c33-28ff-a910-e053-dadaa90a0b859367e7df-b40a-4968-e053-2995a90ae8ac
70859-053-012021-01-29C16284748780-1ba0f9c33-28ff-a910-e053-dadaa90a0b859367e7df-b40a-4968-e053-2995a90ae8ac

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70859-053-01708590053011 KIT in 1 CARTON (70859-053-01) * 1 TUBE in 1 CARTON (51672-1298-1) > 15 g in 1 TUBE * 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0884-0293-01) > 29.57 mL in 1 BOTTLE, WITH APPLICATOR1 kit2019-09-260000-00-00NoNoCurrent