doxycycline
Generic: doxycycline
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
doxycycline
Generic Name
doxycycline
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
doxycycline hyclate 100 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-030
Product ID
71288-030_ccff1290-8098-408e-acf9-2e7d3812959b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218053
Listing Expiration
2026-12-31
Marketing Start
2024-10-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288030
Hyphenated Format
71288-030
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
ANDA218053 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/10mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-030-21) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-030-20)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ccff1290-8098-408e-acf9-2e7d3812959b", "openfda": {"unii": ["19XTS3T51U"], "rxcui": ["310027"], "spl_set_id": ["7772e702-20b3-473a-8bd5-9c7c92e753c6"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (71288-030-21) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-030-20)", "package_ndc": "71288-030-21", "marketing_start_date": "20241028"}], "brand_name": "Doxycycline", "product_id": "71288-030_ccff1290-8098-408e-acf9-2e7d3812959b", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "71288-030", "generic_name": "Doxycycline", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Doxycycline", "active_ingredients": [{"name": "DOXYCYCLINE HYCLATE", "strength": "100 mg/10mL"}], "application_number": "ANDA218053", "marketing_category": "ANDA", "marketing_start_date": "20241028", "listing_expiration_date": "20261231"}