doxycycline hyclate

Generic: doxycycline hyclate

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler major pharmaceuticals
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-0430
Product ID 0904-0430_6f5ebbca-b3a8-4bee-a3c3-1f211b98df88
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 09040430
Hyphenated Format 0904-0430

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
  • 30 BLISTER PACK in 1 CARTON (0904-0430-04) / 1 TABLET, COATED in 1 BLISTER PACK
  • 50 BLISTER PACK in 1 CARTON (0904-0430-06) / 1 TABLET, COATED in 1 BLISTER PACK
  • 20 TABLET, COATED in 1 BOTTLE (0904-0430-95)
source: ndc

Packages (3)

0904-0430-04 30 BLISTER PACK in 1 CARTON (0904-0430-04) / 1 TABLET, COATED in 1 BLISTER PACK 0904-0430-06 50 BLISTER PACK in 1 CARTON (0904-0430-06) / 1 TABLET, COATED in 1 BLISTER PACK 0904-0430-95 20 TABLET, COATED in 1 BOTTLE (0904-0430-95)

Ingredients (1)

doxycycline hyclate (100 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": "6f5ebbca-b3a8-4bee-a3c3-1f211b98df88", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["e7c14a8e-c713-4f03-94e8-1ec9ae077d4d"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-0430-04)  / 1 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "0904-0430-04", "marketing_start_date": "20030702"}, {"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-0430-06)  / 1 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "0904-0430-06", "marketing_start_date": "20030702"}, {"sample": false, "description": "20 TABLET, COATED in 1 BOTTLE (0904-0430-95)", "package_ndc": "0904-0430-95", "marketing_start_date": "20030702"}], "brand_name": "Doxycycline Hyclate", "product_id": "0904-0430_6f5ebbca-b3a8-4bee-a3c3-1f211b98df88", "dosage_form": "TABLET, COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "0904-0430", "generic_name": "Doxycycline hyclate", "labeler_name": "Major Pharmaceuticals", "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"}