doxycycline
Generic: doxycycline
Labeler: mayne pharma inc.Drug Facts
Product Profile
Brand Name
doxycycline
Generic Name
doxycycline
Labeler
mayne pharma inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
doxycycline 40 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68308-668
Product ID
68308-668_4600dc6a-950d-4d84-aed9-da01fbd0db8b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA050805
Listing Expiration
2026-12-31
Marketing Start
2023-02-27
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68308668
Hyphenated Format
68308-668
Supplemental Identifiers
RxCUI
UNII
NUI
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
NDA050805 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (68308-668-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4600dc6a-950d-4d84-aed9-da01fbd0db8b", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["901399"], "spl_set_id": ["0e6b3e17-aeee-4910-8e94-c7ac925b9cca"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Mayne Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (68308-668-30)", "package_ndc": "68308-668-30", "marketing_start_date": "20230227"}], "brand_name": "DOXYCYCLINE", "product_id": "68308-668_4600dc6a-950d-4d84-aed9-da01fbd0db8b", "dosage_form": "CAPSULE", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68308-668", "generic_name": "DOXYCYCLINE", "labeler_name": "Mayne Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "40 mg/1"}], "application_number": "NDA050805", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20230227", "listing_expiration_date": "20261231"}