doxycycline hyclate
Generic: doxyclycline hyclate
Labeler: lupin pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
doxycycline hyclate
Generic Name
doxyclycline hyclate
Labeler
lupin pharmaceuticals, inc.
Dosage Form
TABLET, COATED
Routes
Active Ingredients
doxycycline hyclate 150 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68180654
Hyphenated Format
68180-654
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 150 mg/1
Packaging
- 60 TABLET, COATED in 1 BOTTLE (68180-654-07)
Packages (1)
Ingredients (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"}