doxycycline
Generic: doxycycline
Labeler: fosun pharma usa incDrug Facts
Product Profile
Brand Name
doxycycline
Generic Name
doxycycline
Labeler
fosun pharma usa inc
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
doxycycline hyclate 100 mg/10mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72266237
Hyphenated Format
72266-237
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 100 mg/10mL
Packaging
- 5 VIAL in 1 CARTON (72266-237-05) / 10 mL in 1 VIAL (72266-237-01)
Packages (1)
Ingredients (1)
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"}