doxycycline hyclate

Generic: doxycycline hyclate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7638
Product ID 68788-7638_1f19bdc0-1d90-46be-baf7-c8e73e4b429a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062505
Listing Expiration 2026-12-31
Marketing Start 2020-03-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887638
Hyphenated Format 68788-7638

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 ANDA062505 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 14 TABLET, FILM COATED in 1 BOTTLE (68788-7638-1)
  • 20 TABLET, FILM COATED in 1 BOTTLE (68788-7638-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-7638-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-7638-6)
  • 28 TABLET, FILM COATED in 1 BOTTLE (68788-7638-8)
source: ndc

Packages (5)

68788-7638-1 14 TABLET, FILM COATED in 1 BOTTLE (68788-7638-1) 68788-7638-2 20 TABLET, FILM COATED in 1 BOTTLE (68788-7638-2) 68788-7638-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-7638-3) 68788-7638-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-7638-6) 68788-7638-8 28 TABLET, FILM COATED in 1 BOTTLE (68788-7638-8)

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": "1f19bdc0-1d90-46be-baf7-c8e73e4b429a", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["7646a1cb-537e-4259-bf2a-937ac252a440"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68788-7638-1)", "package_ndc": "68788-7638-1", "marketing_start_date": "20200310"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-7638-2)", "package_ndc": "68788-7638-2", "marketing_start_date": "20200310"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7638-3)", "package_ndc": "68788-7638-3", "marketing_start_date": "20200310"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7638-6)", "package_ndc": "68788-7638-6", "marketing_start_date": "20200310"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68788-7638-8)", "package_ndc": "68788-7638-8", "marketing_start_date": "20200310"}], "brand_name": "Doxycycline Hyclate", "product_id": "68788-7638_1f19bdc0-1d90-46be-baf7-c8e73e4b429a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68788-7638", "generic_name": "Doxycycline Hyclate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062505", "marketing_category": "ANDA", "marketing_start_date": "20200310", "listing_expiration_date": "20261231"}