Minocycline Hydrochloride

Product NDC
55700-415
11-digit product format
557000415
Labeler code
55700
Product ID
55700-415_ef7c40d6-8ad1-498e-b220-4185966c36b3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Minocycline Hydrochloride
Dosage form
CAPSULE
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products 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
2023-12-31
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
55700-415-145570004151414 CAPSULE in 1 BOTTLE (55700-415-14) 14 capsule2016-06-240000-00-00NoNoCurrent
55700-415-205570004152020 CAPSULE in 1 BOTTLE (55700-415-20) 20 capsule2016-06-240000-00-00NoNoCurrent
55700-415-305570004153030 CAPSULE in 1 BOTTLE (55700-415-30) 30 capsule2016-06-240000-00-00NoNoCurrent
55700-415-605570004156060 CAPSULE in 1 BOTTLE (55700-415-60) 60 capsule2017-08-250000-00-00NoNoCurrent