doxycycline hyclate

Generic: doxycycline hyclate

Labeler: cranbury pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler cranbury pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
Cranbury Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 27808-234
Product ID 27808-234_03cb5078-768e-41a1-b922-f1dee98e8760
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211343
Listing Expiration 2026-12-31
Marketing Start 2019-10-09

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 27808234
Hyphenated Format 27808-234

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 ANDA211343 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 50 TABLET in 1 BOTTLE (27808-234-01)
  • 500 TABLET in 1 BOTTLE (27808-234-02)
source: ndc

Packages (2)

27808-234-01 50 TABLET in 1 BOTTLE (27808-234-01) 27808-234-02 500 TABLET in 1 BOTTLE (27808-234-02)

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": "03cb5078-768e-41a1-b922-f1dee98e8760", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["fe6985d2-37f7-4277-94a9-f7125b4b3fd7"], "manufacturer_name": ["Cranbury Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (27808-234-01)", "package_ndc": "27808-234-01", "marketing_start_date": "20220214"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (27808-234-02)", "package_ndc": "27808-234-02", "marketing_start_date": "20220214"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "27808-234_03cb5078-768e-41a1-b922-f1dee98e8760", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "27808-234", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Cranbury Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA211343", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20261231"}