doxycycline hyclate

Generic: doxycycline hyclate

Labeler: sonoma pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate
Generic Name doxycycline hyclate
Labeler sonoma pharmaceuticals, inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

doxycycline hyclate 150 mg/1

Manufacturer
Sonoma Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 69668-515
Product ID 69668-515_6ce404bd-62b7-4aeb-e053-2a91aa0ade68
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207494
Listing Expiration 2026-12-31
Marketing Start 2016-11-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69668515
Hyphenated Format 69668-515

Supplemental Identifiers

RxCUI
799048
UPC
0369668515302
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 ANDA207494 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69668-515-30)
source: ndc

Packages (1)

69668-515-30 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69668-515-30)

Ingredients (1)

doxycycline hyclate (150 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": "6ce404bd-62b7-4aeb-e053-2a91aa0ade68", "openfda": {"upc": ["0369668515302"], "unii": ["19XTS3T51U"], "rxcui": ["799048"], "spl_set_id": ["4fa26176-a730-48ed-9659-e2f64212f418"], "manufacturer_name": ["Sonoma Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (69668-515-30)", "package_ndc": "69668-515-30", "marketing_start_date": "20180510"}], "brand_name": "Doxycycline Hyclate", "product_id": "69668-515_6ce404bd-62b7-4aeb-e053-2a91aa0ade68", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "69668-515", "generic_name": "DOXYCYCLINE HYCLATE", "labeler_name": "Sonoma Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline Hyclate", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "150 mg/1"}], "application_number": "ANDA207494", "marketing_category": "ANDA", "marketing_start_date": "20161128", "listing_expiration_date": "20261231"}