Doxycycline Hyclate

Generic: Doxycycline Hyclate

Labeler: Mayne Pharma Commercial LLC
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Active

Drug Facts

Product Profile

Brand Name Doxycycline Hyclate
Generic Name Doxycycline Hyclate
Labeler Mayne Pharma Commercial LLC
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

DOXYCYCLINE HYCLATE 80 mg/1

Identifiers & Regulatory

Product NDC 51862-571
Product ID 51862-571_add48643-bcf3-4426-b9c1-06fa82b27b78
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA050795
Listing Expiration 2026-12-31
Marketing Start 2020-10-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51862571
Hyphenated Format 51862-571

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 NDA050795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-571-30)
source: ndc

Packages (1)

51862-571-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-571-30)

Ingredients (1)

DOXYCYCLINE HYCLATE (80 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": "add48643-bcf3-4426-b9c1-06fa82b27b78", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["1653433", "2122343"], "spl_set_id": ["f9c63af9-d613-43fc-b8e5-ab6219f24c70"], "manufacturer_name": ["Mayne Pharma Commercial LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-571-30)", "package_ndc": "51862-571-30", "marketing_start_date": "20201002"}], "brand_name": "Doxycycline Hyclate", "product_id": "51862-571_add48643-bcf3-4426-b9c1-06fa82b27b78", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "51862-571", "generic_name": "Doxycycline Hyclate", "labeler_name": "Mayne Pharma Commercial LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "80 mg/1"}], "application_number": "NDA050795", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20201002", "listing_expiration_date": "20261231"}