doxycycline hyclate

Generic: doxycycline hyclate

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler direct rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
direct rx

Identifiers & Regulatory

Product NDC 72189-127
Product ID 72189-127_2be8f93f-be67-aef9-e063-6394a90a547e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062505
Listing Expiration 2026-12-31
Marketing Start 2020-12-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189127
Hyphenated Format 72189-127

Supplemental Identifiers

RxCUI
1650143
UNII
19XTS3T51U

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 ANDA062505 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 14 TABLET, FILM COATED in 1 BOTTLE (72189-127-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE (72189-127-20)
source: ndc

Packages (2)

Ingredients (1)

doxycycline hyclate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be8f93f-be67-aef9-e063-6394a90a547e", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["b56dffde-1334-f5a0-e053-2a95a90a717c"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (72189-127-14)", "package_ndc": "72189-127-14", "marketing_start_date": "20201201"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (72189-127-20)", "package_ndc": "72189-127-20", "marketing_start_date": "20201201"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "72189-127_2be8f93f-be67-aef9-e063-6394a90a547e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72189-127", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062505", "marketing_category": "ANDA", "marketing_start_date": "20201201", "listing_expiration_date": "20261231"}