doxycycline hyclate

Generic: doxycycline hyclate

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler macleods pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-392
Product ID 33342-392_2696f799-7902-4239-807a-9ae85a5d0f1d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211418
Listing Expiration 2027-12-31
Marketing Start 2025-11-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 33342392
Hyphenated Format 33342-392

Supplemental Identifiers

RxCUI
1650143
UPC
0333342392114 0333342392084 0333342392152 0333342392053
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 ANDA211418 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (33342-392-05)
  • 50 TABLET in 1 BOTTLE (33342-392-08)
  • 100 TABLET in 1 BOTTLE (33342-392-11)
  • 10 BLISTER PACK in 1 CARTON (33342-392-12) / 10 TABLET in 1 BLISTER PACK
  • 500 TABLET in 1 BOTTLE (33342-392-15)
source: ndc

Packages (5)

33342-392-05 20 TABLET in 1 BOTTLE (33342-392-05) 33342-392-08 50 TABLET in 1 BOTTLE (33342-392-08) 33342-392-11 100 TABLET in 1 BOTTLE (33342-392-11) 33342-392-12 10 BLISTER PACK in 1 CARTON (33342-392-12) / 10 TABLET in 1 BLISTER PACK 33342-392-15 500 TABLET in 1 BOTTLE (33342-392-15)

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": "2696f799-7902-4239-807a-9ae85a5d0f1d", "openfda": {"upc": ["0333342392114", "0333342392084", "0333342392152", "0333342392053"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["2696f799-7902-4239-807a-9ae85a5d0f1d"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (33342-392-05)", "package_ndc": "33342-392-05", "marketing_start_date": "20251119"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (33342-392-08)", "package_ndc": "33342-392-08", "marketing_start_date": "20251119"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (33342-392-11)", "package_ndc": "33342-392-11", "marketing_start_date": "20251119"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-392-12)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "33342-392-12", "marketing_start_date": "20251119"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (33342-392-15)", "package_ndc": "33342-392-15", "marketing_start_date": "20251119"}], "brand_name": "Doxycycline Hyclate", "product_id": "33342-392_2696f799-7902-4239-807a-9ae85a5d0f1d", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "33342-392", "generic_name": "Doxycycline Hyclate", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA211418", "marketing_category": "ANDA", "marketing_start_date": "20251119", "listing_expiration_date": "20271231"}