doxycycline hyclate

Generic: doxyclycline hyclate

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

Drug Facts

Product Profile

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

doxycycline hyclate 150 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-654
Product ID 68180-654_17750379-d852-4148-be6f-24a101886bf1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208818
Listing Expiration 2026-12-31
Marketing Start 2017-10-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180654
Hyphenated Format 68180-654

Supplemental Identifiers

RxCUI
1649425 1650446
UPC
0368180654070 0368180653073
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 doxyclycline hyclate (source: ndc)
Application Number ANDA208818 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 60 TABLET, COATED in 1 BOTTLE (68180-654-07)
source: ndc

Packages (1)

Ingredients (1)

doxycycline hyclate (150 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "17750379-d852-4148-be6f-24a101886bf1", "openfda": {"upc": ["0368180654070", "0368180653073"], "unii": ["19XTS3T51U"], "rxcui": ["1649425", "1650446"], "spl_set_id": ["f234f419-42da-4a6d-82c6-92106cd77c67"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68180-654-07)", "package_ndc": "68180-654-07", "marketing_start_date": "20171030"}], "brand_name": "doxycycline hyclate", "product_id": "68180-654_17750379-d852-4148-be6f-24a101886bf1", "dosage_form": "TABLET, COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68180-654", "generic_name": "doxyclycline hyclate", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "doxycycline hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "150 mg/1"}], "application_number": "ANDA208818", "marketing_category": "ANDA", "marketing_start_date": "20171030", "listing_expiration_date": "20261231"}