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 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-309
Product ID 72789-309_38052f8d-1d68-b250-e063-6394a90a8b48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065134
Listing Expiration 2026-12-31
Marketing Start 2005-05-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789309
Hyphenated Format 72789-309

Supplemental Identifiers

RxCUI
283535
UPC
0372789309934
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 ANDA065134 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-01)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-60)
  • 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-93)
source: ndc

Packages (3)

72789-309-01 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-01) 72789-309-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-60) 72789-309-93 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-93)

Ingredients (1)

doxycycline hyclate (20 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": "38052f8d-1d68-b250-e063-6394a90a8b48", "openfda": {"upc": ["0372789309934"], "unii": ["19XTS3T51U"], "rxcui": ["283535"], "spl_set_id": ["294c6fc3-e7ca-46ea-b062-a27dd7b0bc97"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-01)", "package_ndc": "72789-309-01", "marketing_start_date": "20230315"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-60)", "package_ndc": "72789-309-60", "marketing_start_date": "20230327"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-309-93)", "package_ndc": "72789-309-93", "marketing_start_date": "20230327"}], "brand_name": "Doxycycline Hyclate", "product_id": "72789-309_38052f8d-1d68-b250-e063-6394a90a8b48", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72789-309", "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": "20 mg/1"}], "application_number": "ANDA065134", "marketing_category": "ANDA", "marketing_start_date": "20050513", "listing_expiration_date": "20261231"}