doxycycline

Generic: doxycycline

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

Drug Facts

Product Profile

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

doxycycline 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-028
Product ID 82804-028_b83c4c4b-2885-43e7-b1c9-0b3bbf75528d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209582
Listing Expiration 2026-12-31
Marketing Start 2018-01-11

Pharmacologic Class

Established (EPC)
tetracycline-class drug [epc]
Chemical Structure
tetracyclines [chemical/ingredient]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804028
Hyphenated Format 82804-028

Supplemental Identifiers

RxCUI
1650142
UPC
0382804028146
UNII
N12000U13O
NUI
N0000175882 N0000007948

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 (source: ndc)
Generic Name doxycycline (source: ndc)
Application Number ANDA209582 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BOTTLE (82804-028-06)
  • 14 TABLET, FILM COATED in 1 BOTTLE (82804-028-14)
  • 20 TABLET, FILM COATED in 1 BOTTLE (82804-028-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (82804-028-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (82804-028-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (82804-028-90)
source: ndc

Packages (6)

Ingredients (1)

doxycycline (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b83c4c4b-2885-43e7-b1c9-0b3bbf75528d", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0382804028146"], "unii": ["N12000U13O"], "rxcui": ["1650142"], "spl_set_id": ["b83c4c4b-2885-43e7-b1c9-0b3bbf75528d"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (82804-028-06)", "package_ndc": "82804-028-06", "marketing_start_date": "20231017"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (82804-028-14)", "package_ndc": "82804-028-14", "marketing_start_date": "20231017"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (82804-028-20)", "package_ndc": "82804-028-20", "marketing_start_date": "20231017"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-028-30)", "package_ndc": "82804-028-30", "marketing_start_date": "20231017"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (82804-028-60)", "package_ndc": "82804-028-60", "marketing_start_date": "20231017"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-028-90)", "package_ndc": "82804-028-90", "marketing_start_date": "20231017"}], "brand_name": "Doxycycline", "product_id": "82804-028_b83c4c4b-2885-43e7-b1c9-0b3bbf75528d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "82804-028", "generic_name": "Doxycycline", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "100 mg/1"}], "application_number": "ANDA209582", "marketing_category": "ANDA", "marketing_start_date": "20180111", "listing_expiration_date": "20261231"}