doxycycline hyclate

Generic: doxycycline hyclate

Labeler: viona pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler viona pharmaceuticals inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Viona Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 72578-001
Product ID 72578-001_6fd4ce71-429d-4bbb-a8e6-afd510319830
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207773
Listing Expiration 2026-12-31
Marketing Start 2019-03-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72578001
Hyphenated Format 72578-001

Supplemental Identifiers

RxCUI
1650143
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 ANDA207773 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72578-001-01)
  • 500 TABLET in 1 BOTTLE (72578-001-05)
  • 1000 TABLET in 1 BOTTLE (72578-001-10)
  • 50 TABLET in 1 BOTTLE (72578-001-18)
  • 10 BLISTER PACK in 1 CARTON (72578-001-77) / 10 TABLET in 1 BLISTER PACK (72578-001-30)
source: ndc

Packages (5)

72578-001-01 100 TABLET in 1 BOTTLE (72578-001-01) 72578-001-05 500 TABLET in 1 BOTTLE (72578-001-05) 72578-001-10 1000 TABLET in 1 BOTTLE (72578-001-10) 72578-001-18 50 TABLET in 1 BOTTLE (72578-001-18) 72578-001-77 10 BLISTER PACK in 1 CARTON (72578-001-77) / 10 TABLET in 1 BLISTER PACK (72578-001-30)

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": "6fd4ce71-429d-4bbb-a8e6-afd510319830", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["763997f0-b35c-43cb-a792-3e0bae589536"], "manufacturer_name": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72578-001-01)", "package_ndc": "72578-001-01", "marketing_start_date": "20190314"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72578-001-05)", "package_ndc": "72578-001-05", "marketing_start_date": "20190314"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72578-001-10)", "package_ndc": "72578-001-10", "marketing_start_date": "20190314"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (72578-001-18)", "package_ndc": "72578-001-18", "marketing_start_date": "20190314"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (72578-001-77)  / 10 TABLET in 1 BLISTER PACK (72578-001-30)", "package_ndc": "72578-001-77", "marketing_start_date": "20190314"}], "brand_name": "Doxycycline Hyclate", "product_id": "72578-001_6fd4ce71-429d-4bbb-a8e6-afd510319830", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72578-001", "generic_name": "Doxycycline Hyclate", "labeler_name": "Viona Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA207773", "marketing_category": "ANDA", "marketing_start_date": "20190314", "listing_expiration_date": "20261231"}