doxycycline hyclate

Generic: doxycycline hyclate

Labeler: jg pharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler jg pharma inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 50 mg/1

Manufacturer
JG Pharma Inc.

Identifiers & Regulatory

Product NDC 72143-211
Product ID 72143-211_74b2de40-77cd-4a58-b648-fbf036f48af0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062269
Marketing Start 2018-04-20
Marketing End 2026-05-31

Pharmacologic Class

Classes
tetracycline-class drug [epc] tetracyclines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72143211
Hyphenated Format 72143-211

Supplemental Identifiers

RxCUI
1652674
UPC
0372143211606
UNII
19XTS3T51U

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 doxycycline hyclate (source: ndc)
Generic Name doxycycline hyclate (source: ndc)
Application Number ANDA062269 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (72143-211-60)
source: ndc

Packages (1)

72143-211-60 60 TABLET, FILM COATED in 1 BOTTLE (72143-211-60)

Ingredients (1)

doxycycline hyclate (50 mg/1)

Linked Drug Pages (1)

Doxycycline Hyclate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "74b2de40-77cd-4a58-b648-fbf036f48af0", "openfda": {"upc": ["0372143211606"], "unii": ["19XTS3T51U"], "rxcui": ["1652674"], "spl_set_id": ["37a8cb92-0ade-4fbc-80f7-2ef283bc32cb"], "manufacturer_name": ["JG Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72143-211-60)", "package_ndc": "72143-211-60", "marketing_end_date": "20260531", "marketing_start_date": "20180420"}], "brand_name": "Doxycycline Hyclate", "product_id": "72143-211_74b2de40-77cd-4a58-b648-fbf036f48af0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72143-211", "generic_name": "Doxycycline Hyclate", "labeler_name": "JG Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "50 mg/1"}], "application_number": "ANDA062269", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20180420"}