doxycycline hyclate

Generic: doxycycline hyclate

Labeler: mayne pharma commercial llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

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 200 mg/1

Manufacturer
Mayne Pharma Commercial LLC

Identifiers & Regulatory

Product NDC 68308-716
Product ID 68308-716_fe12dd75-ce55-4035-9193-0182bc4f5ba6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA050795
Listing Expiration 2026-12-31
Marketing Start 2016-02-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68308716
Hyphenated Format 68308-716

Supplemental Identifiers

RxCUI
406524 434018 799048 1423080
UNII
19XTS3T51U

Packaging Origin

Original Packager
true

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
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-30)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-60)
source: ndc

Packages (2)

68308-716-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-30) 68308-716-60 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-60)

Ingredients (1)

doxycycline hyclate (200 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": "fe12dd75-ce55-4035-9193-0182bc4f5ba6", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["406524", "434018", "799048", "1423080"], "spl_set_id": ["cd2ab9b8-9619-4199-8a5d-83377b3274d1"], "manufacturer_name": ["Mayne Pharma Commercial LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-30)", "package_ndc": "68308-716-30", "marketing_start_date": "20171218"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-60)", "package_ndc": "68308-716-60", "marketing_start_date": "20160201"}], "brand_name": "Doxycycline Hyclate", "product_id": "68308-716_fe12dd75-ce55-4035-9193-0182bc4f5ba6", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68308-716", "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": "200 mg/1"}], "application_number": "NDA050795", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}