minocycline hydrochloride

Generic: minocycline hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name minocycline hydrochloride
Generic Name minocycline hydrochloride
Labeler aurobindo pharma limited
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

minocycline hydrochloride 50 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-209
Product ID 65862-209_2f124ba7-5911-4813-be26-f7f0438d129c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065470
Listing Expiration 2026-12-31
Marketing Start 2008-03-11

Pharmacologic Class

Classes
decreased prothrombin activity [pe] tetracycline-class drug [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862209
Hyphenated Format 65862-209

Supplemental Identifiers

RxCUI
197984 197985 314108
UPC
0365862209054 0365862211057 0365862210050
UNII
0020414E5U

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name minocycline hydrochloride (source: ndc)
Generic Name minocycline hydrochloride (source: ndc)
Application Number ANDA065470 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (65862-209-01)
  • 500 CAPSULE in 1 BOTTLE (65862-209-05)
  • 1000 CAPSULE in 1 BOTTLE (65862-209-99)
source: ndc

Packages (3)

65862-209-01 100 CAPSULE in 1 BOTTLE (65862-209-01) 65862-209-05 500 CAPSULE in 1 BOTTLE (65862-209-05) 65862-209-99 1000 CAPSULE in 1 BOTTLE (65862-209-99)

Ingredients (1)

minocycline hydrochloride (50 mg/1)

Linked Drug Pages (1)

Minocycline Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f124ba7-5911-4813-be26-f7f0438d129c", "openfda": {"upc": ["0365862209054", "0365862211057", "0365862210050"], "unii": ["0020414E5U"], "rxcui": ["197984", "197985", "314108"], "spl_set_id": ["9013ca48-15f2-43cd-a51d-91cf65c72a7c"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (65862-209-01)", "package_ndc": "65862-209-01", "marketing_start_date": "20080311"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (65862-209-05)", "package_ndc": "65862-209-05", "marketing_start_date": "20080311"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (65862-209-99)", "package_ndc": "65862-209-99", "marketing_start_date": "20080311"}], "brand_name": "Minocycline Hydrochloride", "product_id": "65862-209_2f124ba7-5911-4813-be26-f7f0438d129c", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Prothrombin Activity [PE]", "Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "65862-209", "generic_name": "Minocycline Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Minocycline Hydrochloride", "active_ingredients": [{"name": "MINOCYCLINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA065470", "marketing_category": "ANDA", "marketing_start_date": "20080311", "listing_expiration_date": "20261231"}