doxycycline
Generic: doxycycline
Labeler: lupin pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
doxycycline
Generic Name
doxycycline
Labeler
lupin pharmaceuticals, inc.
Dosage Form
FOR SUSPENSION
Routes
Active Ingredients
doxycycline 25 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68180-657
Product ID
68180-657_6e5c9f41-4304-4121-845f-b894a4fd5d95
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201678
Listing Expiration
2026-12-31
Marketing Start
2013-06-11
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68180657
Hyphenated Format
68180-657
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
ANDA201678 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/5mL
Packaging
- 60 mL in 1 BOTTLE (68180-657-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6e5c9f41-4304-4121-845f-b894a4fd5d95", "openfda": {"nui": ["N0000175882", "N0000007948"], "unii": ["N12000U13O"], "rxcui": ["1650030"], "spl_set_id": ["e0e80435-1b6a-4361-8c8a-e432f8f23a1b"], "pharm_class_cs": ["Tetracyclines [Chemical/Ingredient]"], "pharm_class_epc": ["Tetracycline-class Drug [EPC]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE (68180-657-01)", "package_ndc": "68180-657-01", "marketing_start_date": "20130611"}], "brand_name": "DOXYCYCLINE", "product_id": "68180-657_6e5c9f41-4304-4121-845f-b894a4fd5d95", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Tetracycline-class Drug [EPC]", "Tetracyclines [CS]"], "product_ndc": "68180-657", "generic_name": "DOXYCYCLINE", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOXYCYCLINE", "active_ingredients": [{"name": "DOXYCYCLINE", "strength": "25 mg/5mL"}], "application_number": "ANDA201678", "marketing_category": "ANDA", "marketing_start_date": "20130611", "listing_expiration_date": "20261231"}