doxycycline

Generic: doxycycline

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name doxycycline
Generic Name doxycycline
Labeler endo usa, inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

doxycycline hyclate 100 mg/10mL

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 42023-244
Product ID 42023-244_d3631394-b84d-4dc2-b870-e7c3aa2573b4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216690
Listing Expiration 2026-12-31
Marketing Start 2024-11-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42023244
Hyphenated Format 42023-244

Supplemental Identifiers

RxCUI
310027
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 (source: ndc)
Generic Name doxycycline (source: ndc)
Application Number ANDA216690 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/10mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (42023-244-10) / 10 mL in 1 VIAL (42023-244-01)
source: ndc

Packages (1)

Ingredients (1)

doxycycline hyclate (100 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d3631394-b84d-4dc2-b870-e7c3aa2573b4", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["310027"], "spl_set_id": ["acb84610-5e26-4b0c-89e5-42bc0f8fa00d"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (42023-244-10)  / 10 mL in 1 VIAL (42023-244-01)", "package_ndc": "42023-244-10", "marketing_start_date": "20241126"}], "brand_name": "DOXYCYCLINE", "product_id": "42023-244_d3631394-b84d-4dc2-b870-e7c3aa2573b4", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "42023-244", "generic_name": "Doxycycline", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/10mL"}], "application_number": "ANDA216690", "marketing_category": "ANDA", "marketing_start_date": "20241126", "listing_expiration_date": "20261231"}