doxycycline hyclate

Generic: doxycycline hyclate

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1104
Product ID 70771-1104_6a571164-83bf-4150-a6b7-9d059793a933
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207773
Listing Expiration 2026-12-31
Marketing Start 2018-04-02

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711104
Hyphenated Format 70771-1104

Supplemental Identifiers

RxCUI
1650143
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 ANDA207773 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (70771-1104-0)
  • 100 TABLET in 1 BOTTLE (70771-1104-1)
  • 10 BLISTER PACK in 1 CARTON (70771-1104-4) / 10 TABLET in 1 BLISTER PACK (70771-1104-2)
  • 500 TABLET in 1 BOTTLE (70771-1104-5)
  • 50 TABLET in 1 BOTTLE (70771-1104-7)
source: ndc

Packages (5)

70771-1104-0 1000 TABLET in 1 BOTTLE (70771-1104-0) 70771-1104-1 100 TABLET in 1 BOTTLE (70771-1104-1) 70771-1104-4 10 BLISTER PACK in 1 CARTON (70771-1104-4) / 10 TABLET in 1 BLISTER PACK (70771-1104-2) 70771-1104-5 500 TABLET in 1 BOTTLE (70771-1104-5) 70771-1104-7 50 TABLET in 1 BOTTLE (70771-1104-7)

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": "6a571164-83bf-4150-a6b7-9d059793a933", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["68b3aba5-f1e4-4cdf-b244-0302aa8595fe"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1104-0)", "package_ndc": "70771-1104-0", "marketing_start_date": "20180402"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1104-1)", "package_ndc": "70771-1104-1", "marketing_start_date": "20180402"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1104-4)  / 10 TABLET in 1 BLISTER PACK (70771-1104-2)", "package_ndc": "70771-1104-4", "marketing_start_date": "20180402"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1104-5)", "package_ndc": "70771-1104-5", "marketing_start_date": "20180402"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (70771-1104-7)", "package_ndc": "70771-1104-7", "marketing_start_date": "20180402"}], "brand_name": "Doxycycline hyclate", "product_id": "70771-1104_6a571164-83bf-4150-a6b7-9d059793a933", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70771-1104", "generic_name": "Doxycycline hyclate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA207773", "marketing_category": "ANDA", "marketing_start_date": "20180402", "listing_expiration_date": "20261231"}