doxycycline hyclate delayed release

Generic: doxycycline hyclate

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline hyclate delayed release
Generic Name doxycycline hyclate
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

doxycycline hyclate 150 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-143
Product ID 23155-143_74ed8d09-3486-4f4f-8df1-ea8f9f380741
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200856
Listing Expiration 2026-12-31
Marketing Start 2013-04-30

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155143
Hyphenated Format 23155-143

Supplemental Identifiers

RxCUI
406524 434018 799048 1423080
UPC
0323155611069 0323155141016 0323155142013
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 delayed release (source: ndc)
Generic Name doxycycline hyclate (source: ndc)
Application Number ANDA200856 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-01)
  • 250 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-04)
  • 60 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-06)
source: ndc

Packages (3)

23155-143-01 100 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-01) 23155-143-04 250 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-04) 23155-143-06 60 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-06)

Ingredients (1)

doxycycline hyclate (150 mg/1)

Linked Drug Pages (1)

DOXYCYCLINE HYCLATE DELAYED RELEASE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "74ed8d09-3486-4f4f-8df1-ea8f9f380741", "openfda": {"upc": ["0323155611069", "0323155141016", "0323155142013"], "unii": ["19XTS3T51U"], "rxcui": ["406524", "434018", "799048", "1423080"], "spl_set_id": ["f5ee43b2-d6ca-4819-a3d7-07f8421015d7"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-01)", "package_ndc": "23155-143-01", "marketing_start_date": "20130430"}, {"sample": false, "description": "250 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-04)", "package_ndc": "23155-143-04", "marketing_start_date": "20130430"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-143-06)", "package_ndc": "23155-143-06", "marketing_start_date": "20130430"}], "brand_name": "DOXYCYCLINE HYCLATE DELAYED RELEASE", "product_id": "23155-143_74ed8d09-3486-4f4f-8df1-ea8f9f380741", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "23155-143", "generic_name": "doxycycline hyclate", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE HYCLATE", "brand_name_suffix": "DELAYED RELEASE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "150 mg/1"}], "application_number": "ANDA200856", "marketing_category": "ANDA", "marketing_start_date": "20130430", "listing_expiration_date": "20261231"}