DYNACIN

Product NDC
49884-096
11-digit product format
498840096
Labeler code
49884
Product ID
49884-096_3bb7df02-5222-4765-b0ba-2a7c8f41e98d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Minocycline Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Par Pharmaceutical, Inc.
Application
ANDA065131
Marketing category
ANDA
Marketing start
2011-06-20
Marketing end
0000-00-00
Substance
MINOCYCLINE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Tetracycline-class Drug [EPC],Tetracyclines [CS]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49884-096-012025-02-05C16284748780-19d75b9d0-bdf7-f424-e053-dadaa90a57cef174edbd-3ac0-4e27-a116-3b74804721bb
49884-096-012020-01-31C16284748780-19d75b9d0-bdf7-f424-e053-dadaa90a57cef174edbd-3ac0-4e27-a116-3b74804721bb

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49884-096-01EA - Each49884-0961d415f81-33d2-4266-8ad2-44baa29c8e0612013-02-13