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
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-173
Product ID 82804-173_9f066753-55e4-4cf7-b4ec-225170fec1cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062421
Listing Expiration 2026-12-31
Marketing Start 1990-01-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804173
Hyphenated Format 82804-173

Supplemental Identifiers

RxCUI
1650143
UPC
0382804173143
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 ANDA062421 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 14 TABLET in 1 BOTTLE, PLASTIC (82804-173-14)
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": "9f066753-55e4-4cf7-b4ec-225170fec1cb", "openfda": {"upc": ["0382804173143"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["19d93cd3-6ac6-4e5d-8e7e-1a48799df3cf"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (82804-173-14)", "package_ndc": "82804-173-14", "marketing_start_date": "20241212"}], "brand_name": "Doxycycline Hyclate", "product_id": "82804-173_9f066753-55e4-4cf7-b4ec-225170fec1cb", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "82804-173", "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": "ANDA062421", "marketing_category": "ANDA", "marketing_start_date": "19900101", "listing_expiration_date": "20261231"}