doxycycline hyclate

Generic: doxycycline hyclate

Labeler: qpharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler qpharma, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
QPharma, Inc.

Identifiers & Regulatory

Product NDC 42708-173
Product ID 42708-173_46827da0-577c-60e7-e063-6294a90a99e7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065095
Listing Expiration 2026-12-31
Marketing Start 2003-07-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42708173
Hyphenated Format 42708-173

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 ANDA065095 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 20 TABLET, COATED in 1 BOTTLE, PLASTIC (42708-173-20)
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": "46827da0-577c-60e7-e063-6294a90a99e7", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["fbd0a22f-b365-c0a2-e053-6394a90a1e07"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "20 TABLET, COATED in 1 BOTTLE, PLASTIC (42708-173-20)", "package_ndc": "42708-173-20", "marketing_start_date": "20230519"}], "brand_name": "Doxycycline Hyclate", "product_id": "42708-173_46827da0-577c-60e7-e063-6294a90a99e7", "dosage_form": "TABLET, COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "42708-173", "generic_name": "Doxycycline Hyclate", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA065095", "marketing_category": "ANDA", "marketing_start_date": "20030702", "listing_expiration_date": "20261231"}