Minocycline hydrochloride

Product NDC
63629-2796
11-digit product format
636292796
Labeler code
63629
Product ID
63629-2796_b2a38b76-cf60-4e84-8627-c9f489d6d901
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Minocycline hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA065062
Marketing category
ANDA
Marketing start
2000-12-22
Marketing end
0000-00-00
Substance
MINOCYCLINE HYDROCHLORIDE
Active strength
50 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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
0020414E5UMINOCYCLINE HYDROCHLORIDE13614-98-7MINOCYCLINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-2796-16362927960190 CAPSULE in 1 BOTTLE (63629-2796-1) 90 capsule2010-09-290000-00-00NoNoCurrent
63629-2796-26362927960250 CAPSULE in 1 BOTTLE (63629-2796-2) 50 capsule2010-09-290000-00-00NoNoCurrent
63629-2796-36362927960360 CAPSULE in 1 BOTTLE (63629-2796-3) 60 capsule2010-09-290000-00-00NoNoCurrent
63629-2796-46362927960430 CAPSULE in 1 BOTTLE (63629-2796-4) 30 capsule2010-09-290000-00-00NoNoCurrent
63629-2796-563629279605100 CAPSULE in 1 BOTTLE (63629-2796-5) 100 capsule2010-09-290000-00-00NoNoCurrent