doxycycline hyclate

Generic: doxycycline hyclate

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

doxycycline hyclate 100 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-279
Product ID 50268-279_461626eb-97e0-bb4c-e063-6394a90a10c5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062677
Listing Expiration 2026-12-31
Marketing Start 2014-06-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268279
Hyphenated Format 50268-279

Supplemental Identifiers

RxCUI
1649405 1649988 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 ANDA062677 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-279-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-279-11)
source: ndc

Packages (1)

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": "461626eb-97e0-bb4c-e063-6394a90a10c5", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1649405", "1649988", "1650143"], "spl_set_id": ["53ff9f7e-0db0-c841-d334-4cf31f658828"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-279-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-279-11)", "package_ndc": "50268-279-15", "marketing_start_date": "20140604"}], "brand_name": "Doxycycline Hyclate", "product_id": "50268-279_461626eb-97e0-bb4c-e063-6394a90a10c5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "50268-279", "generic_name": "Doxycycline Hyclate", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062677", "marketing_category": "ANDA", "marketing_start_date": "20140604", "listing_expiration_date": "20261231"}