FDA.reportPublic FDA data

Minocycline Hydrochloride

Product NDC
63629-9212
11-digit product format
636299212
Labeler code
63629
Product ID
63629-9212_b98efaa3-1ba0-46c6-bb61-5bd83968339c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Minocycline Hydrochloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA204453
Marketing category
ANDA
Marketing start
2019-12-23
Substance
MINOCYCLINE HYDROCHLORIDE
Active strength
55 mg/1
Pharmacologic classes
Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Minocycline Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MINOCYCLINE HYDROCHLORIDE55 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0020414E5U
Rxcui1013662

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d9c90ddb-dcc8-42af-a94b-505e4488bdc7Product name120250623
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9e423e97-a6d9-7bb0-0dcb-343af7c0ff92Product name220230322
472a6924-c7ed-850b-32ce-a510e887fbf9Product name420230207
f1239550-2d2e-44c3-aec7-14fd9b4ab55dProduct name120201103
7a57513a-a145-4b95-9165-1e0ef21d6017Product name120200326
70555e58-6951-4421-9354-f80c6ce0d92cProduct name720200204
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
23de08d7-aa4e-ec8b-ce6d-2124a855e4efProduct name520180605
76736e48-254d-4a39-993d-206efbdaad1dProduct name120170717
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
0c498039-5512-d9d7-e6b6-833de47219ffProduct name220151106
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
d723478e-ad4a-ec23-6bd7-cfe33e1e3840Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63629-9212-1Minocycline Hydrochloride30 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE30106

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-9212-1EA - Each63629-9212d53d51d1-ef93-4db6-90fb-f190b710e73e12022-04-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63629-9212MINOCYCLINE HYDROCHLORIDE TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]105Current NDC, Legacy NDC, 1 package rows20240915_a0f88292-680b-4d50-ae6e-0a7bccc3a9c6.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1013662minocycline HCl 55 MG 24HR Extended Release Oral TabletPSNa0f88292-680b-4d50-ae6e-0a7bccc3a9c6106
101366224 HR minocycline 55 MG Extended Release Oral TabletSCDa0f88292-680b-4d50-ae6e-0a7bccc3a9c6106
1013662minocycline 55 MG 24 HR Extended Release Oral TabletSYa0f88292-680b-4d50-ae6e-0a7bccc3a9c6106

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63629-9212-16362992120130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9212-1) 2022-03-020000-00-00NoNoCurrent