doxycycline hyclate

Generic: doxycycline hyclate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

doxycycline hyclate 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-697
Product ID 71205-697_dd7672c9-b10f-4ea1-9000-ef3e3faa10db
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062505
Listing Expiration 2026-12-31
Marketing Start 1984-09-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205697
Hyphenated Format 71205-697

Supplemental Identifiers

RxCUI
1650143
UPC
0371205697204
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
  • 10 TABLET, FILM COATED in 1 BOTTLE (71205-697-10)
  • 14 TABLET, FILM COATED in 1 BOTTLE (71205-697-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE (71205-697-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-697-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-697-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-697-90)
source: ndc

Packages (6)

71205-697-10 10 TABLET, FILM COATED in 1 BOTTLE (71205-697-10) 71205-697-14 14 TABLET, FILM COATED in 1 BOTTLE (71205-697-14) 71205-697-20 20 TABLET, FILM COATED in 1 BOTTLE (71205-697-20) 71205-697-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-697-30) 71205-697-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-697-60) 71205-697-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-697-90)

Ingredients (1)

doxycycline hyclate (100 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": "dd7672c9-b10f-4ea1-9000-ef3e3faa10db", "openfda": {"upc": ["0371205697204"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["dd7672c9-b10f-4ea1-9000-ef3e3faa10db"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-697-10)", "package_ndc": "71205-697-10", "marketing_start_date": "20220914"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (71205-697-14)", "package_ndc": "71205-697-14", "marketing_start_date": "20220914"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-697-20)", "package_ndc": "71205-697-20", "marketing_start_date": "20220914"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-697-30)", "package_ndc": "71205-697-30", "marketing_start_date": "20220914"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-697-60)", "package_ndc": "71205-697-60", "marketing_start_date": "20220914"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-697-90)", "package_ndc": "71205-697-90", "marketing_start_date": "20220914"}], "brand_name": "Doxycycline Hyclate", "product_id": "71205-697_dd7672c9-b10f-4ea1-9000-ef3e3faa10db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "71205-697", "generic_name": "Doxycycline Hyclate", "labeler_name": "Proficient Rx LP", "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": "19840911", "listing_expiration_date": "20261231"}