doxycycline hyclate

Generic: doxycycline hyclate

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

doxycycline hyclate 20 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-623
Product ID 62135-623_32d032a2-c17d-4b61-e063-6394a90a9a95
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065277
Listing Expiration 2026-12-31
Marketing Start 2005-11-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135623
Hyphenated Format 62135-623

Supplemental Identifiers

RxCUI
283535
UPC
0362135623906
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 ANDA065277 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (62135-623-90)
source: ndc

Packages (1)

Ingredients (1)

doxycycline hyclate (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32d032a2-c17d-4b61-e063-6394a90a9a95", "openfda": {"upc": ["0362135623906"], "unii": ["19XTS3T51U"], "rxcui": ["283535"], "spl_set_id": ["b3294889-e8f8-42f1-9bd0-13d87572997a"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62135-623-90)", "package_ndc": "62135-623-90", "marketing_start_date": "20230220"}], "brand_name": "Doxycycline Hyclate", "product_id": "62135-623_32d032a2-c17d-4b61-e063-6394a90a9a95", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "62135-623", "generic_name": "Doxycycline Hyclate", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "20 mg/1"}], "application_number": "ANDA065277", "marketing_category": "ANDA", "marketing_start_date": "20051110", "listing_expiration_date": "20261231"}