doxycycline hyclate

Generic: doxycycline hyclate

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

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler actavis pharma, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

doxycycline hyclate 200 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0591-4575
Product ID 0591-4575_d2422c7a-2c5f-4377-8828-2f53f09a7246
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090134
Listing Expiration 2026-12-31
Marketing Start 2019-08-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05914575
Hyphenated Format 0591-4575

Supplemental Identifiers

RxCUI
1423080 1653433
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 ANDA090134 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (0591-4575-60)
source: ndc

Packages (1)

0591-4575-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (0591-4575-60)

Ingredients (1)

doxycycline hyclate (200 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": "d2422c7a-2c5f-4377-8828-2f53f09a7246", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1423080", "1653433"], "spl_set_id": ["c2b08332-3256-4658-965a-ede3d973a388"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (0591-4575-60)", "package_ndc": "0591-4575-60", "marketing_start_date": "20190814"}], "brand_name": "Doxycycline Hyclate", "product_id": "0591-4575_d2422c7a-2c5f-4377-8828-2f53f09a7246", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0591-4575", "generic_name": "Doxycycline Hyclate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "200 mg/1"}], "application_number": "ANDA090134", "marketing_category": "ANDA", "marketing_start_date": "20190814", "listing_expiration_date": "20261231"}