doxycycline hyclate

Generic: doxycycline hyclate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

doxycycline hyclate 100 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-319
Product ID 72789-319_38058bd8-226e-5aca-e063-6294a90a32f8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA062677
Listing Expiration 2026-12-31
Marketing Start 1986-07-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789319
Hyphenated Format 72789-319

Supplemental Identifiers

RxCUI
1650143
UPC
0372789319100
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 ANDA062677 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-06)
  • 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-07)
  • 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-10)
  • 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-14)
  • 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-28)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-60)
source: ndc

Packages (7)

Ingredients (1)

doxycycline hyclate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38058bd8-226e-5aca-e063-6294a90a32f8", "openfda": {"upc": ["0372789319100"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["3af9348c-a98b-4059-a5ef-4229e2b33af0"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-06)", "package_ndc": "72789-319-06", "marketing_start_date": "20231218"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-07)", "package_ndc": "72789-319-07", "marketing_start_date": "20231206"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-10)", "package_ndc": "72789-319-10", "marketing_start_date": "20230329"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-14)", "package_ndc": "72789-319-14", "marketing_start_date": "20250404"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-28)", "package_ndc": "72789-319-28", "marketing_start_date": "20230426"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-30)", "package_ndc": "72789-319-30", "marketing_start_date": "20230808"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-319-60)", "package_ndc": "72789-319-60", "marketing_start_date": "20230606"}], "brand_name": "Doxycycline Hyclate", "product_id": "72789-319_38058bd8-226e-5aca-e063-6294a90a32f8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72789-319", "generic_name": "Doxycycline Hyclate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062677", "marketing_category": "ANDA", "marketing_start_date": "19860710", "listing_expiration_date": "20261231"}