doxycycline

Generic: doxycycline

Labeler: fosun pharma usa inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

doxycycline hyclate 100 mg/10mL

Manufacturer
FOSUN PHARMA USA INC

Identifiers & Regulatory

Product NDC 72266-237
Product ID 72266-237_31ba285b-5aef-ff76-e063-6294a90a9321
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215583
Listing Expiration 2026-12-31
Marketing Start 2023-04-12

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72266237
Hyphenated Format 72266-237

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 ANDA215583 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/10mL
source: ndc
Packaging
  • 5 VIAL in 1 CARTON (72266-237-05) / 10 mL in 1 VIAL (72266-237-01)
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": "31ba285b-5aef-ff76-e063-6294a90a9321", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["310027"], "spl_set_id": ["fa3fbb09-b830-60c5-e053-6394a90a4165"], "manufacturer_name": ["FOSUN PHARMA USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (72266-237-05)  / 10 mL in 1 VIAL (72266-237-01)", "package_ndc": "72266-237-05", "marketing_start_date": "20230412"}], "brand_name": "DOXYCYCLINE", "product_id": "72266-237_31ba285b-5aef-ff76-e063-6294a90a9321", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "72266-237", "generic_name": "DOXYCYCLINE", "labeler_name": "FOSUN PHARMA USA INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/10mL"}], "application_number": "ANDA215583", "marketing_category": "ANDA", "marketing_start_date": "20230412", "listing_expiration_date": "20261231"}