Minocycline Hydrochloride

Product NDC
58118-0484
11-digit product format
581180484
Labeler code
58118
Product ID
58118-0484_ae6a8939-d57d-f441-e053-2995a90aad7c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Minocycline Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Clinical Solutions Wholesale, LLC
Application
ANDA065062
Marketing category
ANDA
Marketing start
2015-04-02
Marketing end
0000-00-00
Substance
MINOCYCLINE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC],Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58118-0484-82024-01-30C16284748780-11030e365-5ebc-111a-e063-dadaa90a10e27813e930-2cca-42be-b1b2-c5fc86040cf3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58118-0484MINOCYCLINE HYDROCHLORIDE CAPSULE [CLINICAL SOLUTIONS WHOLESALE, LLC]7Legacy NDC20200904_7813e930-2cca-42be-b1b2-c5fc86040cf3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58118-0484-85811804840830 CAPSULE in 1 BLISTER PACK (58118-0484-8) 30 capsule2016-07-050000-00-00NoNoCurrent