doxycycline hyclate
Generic: doxycycline hyclate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
doxycycline hyclate
Generic Name
doxycycline hyclate
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
doxycycline hyclate 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3213
Product ID
70518-3213_4ab5f236-de3c-3af3-e063-6394a90a6ff5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA062677
Listing Expiration
2027-12-31
Marketing Start
2021-09-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183213
Hyphenated Format
70518-3213
Supplemental Identifiers
RxCUI
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
ANDA062677 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3213-1)
- 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3213-6)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ab5f236-de3c-3af3-e063-6394a90a6ff5", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["c8194d6e-c407-465e-a342-4d2d9756dfc4"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3213-1)", "package_ndc": "70518-3213-1", "marketing_start_date": "20230625"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3213-6)", "package_ndc": "70518-3213-6", "marketing_start_date": "20250430"}], "brand_name": "Doxycycline Hyclate", "product_id": "70518-3213_4ab5f236-de3c-3af3-e063-6394a90a6ff5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-3213", "generic_name": "Doxycycline Hyclate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/1"}], "application_number": "ANDA062677", "marketing_category": "ANDA", "marketing_start_date": "20210908", "listing_expiration_date": "20271231"}