doxycycline

Generic: doxycycline

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
Generic Name doxycycline
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

doxycycline 150 mg/1

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

Identifiers & Regulatory

Product NDC 23155-136
Product ID 23155-136_ec6854e5-3f41-4b8f-be77-49e3bd19f7c4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091605
Listing Expiration 2026-12-31
Marketing Start 2012-05-01

Pharmacologic Class

Established (EPC)
tetracycline-class drug [epc]
Chemical Structure
tetracyclines [chemical/ingredient]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155136
Hyphenated Format 23155-136

Supplemental Identifiers

RxCUI
1649429 1650142 1650444 1652673
UPC
0323155135053
UNII
N12000U13O
NUI
N0000175882 N0000007948

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 (source: ndc)
Generic Name doxycycline (source: ndc)
Application Number ANDA091605 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (23155-136-03)
  • 500 TABLET in 1 BOTTLE (23155-136-05)
  • 10 TABLET in 1 BLISTER PACK (23155-136-11)
  • 30 TABLET in 1 CARTON (23155-136-30)
source: ndc

Packages (4)

23155-136-03 30 TABLET in 1 BOTTLE (23155-136-03) 23155-136-05 500 TABLET in 1 BOTTLE (23155-136-05) 23155-136-11 10 TABLET in 1 BLISTER PACK (23155-136-11) 23155-136-30 30 TABLET in 1 CARTON (23155-136-30)

Ingredients (1)

doxycycline (150 mg/1)

Linked Drug Pages (1)

Doxycycline ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ec6854e5-3f41-4b8f-be77-49e3bd19f7c4", "openfda": {"nui": ["N0000175882", "N0000007948"], "upc": ["0323155135053"], "unii": ["N12000U13O"], "rxcui": ["1649429", "1650142", "1650444", "1652673"], "spl_set_id": ["2bcde264-5f6f-47f6-ae2e-1b7010deacf7"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (23155-136-03)", "package_ndc": "23155-136-03", "marketing_start_date": "20120501"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-136-05)", "package_ndc": "23155-136-05", "marketing_start_date": "20120501"}, {"sample": false, "description": "10 TABLET in 1 BLISTER PACK (23155-136-11)", "package_ndc": "23155-136-11", "marketing_start_date": "20120501"}, {"sample": false, "description": "30 TABLET in 1 CARTON (23155-136-30)", "package_ndc": "23155-136-30", "marketing_start_date": "20120501"}], "brand_name": "Doxycycline", "product_id": "23155-136_ec6854e5-3f41-4b8f-be77-49e3bd19f7c4", "dosage_form": "TABLET", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "23155-136", "generic_name": "Doxycycline", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "150 mg/1"}], "application_number": "ANDA091605", "marketing_category": "ANDA", "marketing_start_date": "20120501", "listing_expiration_date": "20261231"}