Minocycline hydrochloride

Product NDC
33261-434
11-digit product format
332610434
Labeler code
33261
Product ID
33261-434_b467b2f6-9ecd-45be-a714-664764233d01
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Minocycline hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Aidarex Pharmaceuticals LLC
Application
ANDA065062
Marketing category
ANDA
Marketing start
2000-12-22
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
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

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

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
MINOCYCLINE HCL 50MG 100MG CAP RANBAXY AND OHMAidarex Pharmaceuticals LLC2014-01-14HUMAN PRESCRIPTION DRUG LABEL1