doxycycline hyclate

Generic: doxycycline hyclate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxycycline hyclate 100 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3869
Product ID 70518-3869_4986e936-79e7-6ab8-e063-6394a90ab0d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211343
Listing Expiration 2027-12-31
Marketing Start 2023-09-24

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183869
Hyphenated Format 70518-3869

Supplemental Identifiers

RxCUI
1650143
UNII
19XTS3T51U

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
  • 20 TABLET in 1 BOTTLE, PLASTIC (70518-3869-0)
  • 14 TABLET in 1 BOTTLE, PLASTIC (70518-3869-2)
  • 60 TABLET in 1 BOTTLE, PLASTIC (70518-3869-4)
  • 100 TABLET in 1 BOTTLE, PLASTIC (70518-3869-5)
  • 28 TABLET in 1 BOTTLE, PLASTIC (70518-3869-6)
  • 50 TABLET in 1 BOTTLE, PLASTIC (70518-3869-7)
  • 56 TABLET in 1 BOTTLE, PLASTIC (70518-3869-8)
  • 30 TABLET in 1 BLISTER PACK (70518-3869-9)
source: ndc

Packages (8)

70518-3869-0 20 TABLET in 1 BOTTLE, PLASTIC (70518-3869-0) 70518-3869-2 14 TABLET in 1 BOTTLE, PLASTIC (70518-3869-2) 70518-3869-4 60 TABLET in 1 BOTTLE, PLASTIC (70518-3869-4) 70518-3869-5 100 TABLET in 1 BOTTLE, PLASTIC (70518-3869-5) 70518-3869-6 28 TABLET in 1 BOTTLE, PLASTIC (70518-3869-6) 70518-3869-7 50 TABLET in 1 BOTTLE, PLASTIC (70518-3869-7) 70518-3869-8 56 TABLET in 1 BOTTLE, PLASTIC (70518-3869-8) 70518-3869-9 30 TABLET in 1 BLISTER PACK (70518-3869-9)

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": "4986e936-79e7-6ab8-e063-6394a90ab0d4", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1650143"], "spl_set_id": ["5fdc01c3-c62f-40cf-8351-91cbcc43d379"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (70518-3869-0)", "package_ndc": "70518-3869-0", "marketing_start_date": "20230924"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (70518-3869-2)", "package_ndc": "70518-3869-2", "marketing_start_date": "20231108"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-3869-4)", "package_ndc": "70518-3869-4", "marketing_start_date": "20250302"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-3869-5)", "package_ndc": "70518-3869-5", "marketing_start_date": "20250330"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (70518-3869-6)", "package_ndc": "70518-3869-6", "marketing_start_date": "20250421"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (70518-3869-7)", "package_ndc": "70518-3869-7", "marketing_start_date": "20250714"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE, PLASTIC (70518-3869-8)", "package_ndc": "70518-3869-8", "marketing_start_date": "20250714"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3869-9)", "package_ndc": "70518-3869-9", "marketing_start_date": "20250821"}], "brand_name": "DOXYCYCLINE HYCLATE", "product_id": "70518-3869_4986e936-79e7-6ab8-e063-6394a90ab0d4", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "70518-3869", "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": "ANDA211343", "marketing_category": "ANDA", "marketing_start_date": "20230924", "listing_expiration_date": "20271231"}