doxycycline hyclate
Generic: doxycycline hyclate
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
doxycycline hyclate
Generic Name
doxycycline hyclate
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
doxycycline hyclate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-4836
Product ID
68071-4836_1ae175c6-5f09-8a7a-e063-6294a90a6461
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062269
Listing Expiration
2026-12-31
Marketing Start
2016-10-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680714836
Hyphenated Format
68071-4836
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA062269 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 10 TABLET, FILM COATED in 1 BOTTLE (68071-4836-1)
- 14 TABLET, FILM COATED in 1 BOTTLE (68071-4836-7)
- 28 TABLET, FILM COATED in 1 BOTTLE (68071-4836-8)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ae175c6-5f09-8a7a-e063-6294a90a6461", "openfda": {"upc": ["0368071483680"], "unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["860a1566-5857-ed88-e053-2991aa0ae2a4"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68071-4836-1)", "package_ndc": "68071-4836-1", "marketing_start_date": "20190408"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68071-4836-7)", "package_ndc": "68071-4836-7", "marketing_start_date": "20190408"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68071-4836-8)", "package_ndc": "68071-4836-8", "marketing_start_date": "20190408"}], "brand_name": "Doxycycline Hyclate", "product_id": "68071-4836_1ae175c6-5f09-8a7a-e063-6294a90a6461", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68071-4836", "generic_name": "Doxycycline Hyclate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062269", "marketing_category": "ANDA", "marketing_start_date": "20161001", "listing_expiration_date": "20261231"}