latanoprost
Generic: latanoprost
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
latanoprost
Generic Name
latanoprost
Labeler
rising pharma holdings, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
latanoprost 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
64980-516
Product ID
64980-516_c9d37a89-f385-4cd5-9a18-15abc5ba2dd9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202442
Listing Expiration
2026-12-31
Marketing Start
2016-09-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64980516
Hyphenated Format
64980-516
Supplemental Identifiers
RxCUI
UPC
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
latanoprost (source: ndc)
Generic Name
latanoprost (source: ndc)
Application Number
ANDA202442 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 1 BOTTLE, DROPPER in 1 CARTON (64980-516-25) / 2.5 mL in 1 BOTTLE, DROPPER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "c9d37a89-f385-4cd5-9a18-15abc5ba2dd9", "openfda": {"nui": ["N0000175454", "M0017805"], "upc": ["0364980516259"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["e25b82a9-1b04-4b40-8472-be107a2a6731"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (64980-516-25) / 2.5 mL in 1 BOTTLE, DROPPER", "package_ndc": "64980-516-25", "marketing_start_date": "20160901"}], "brand_name": "LATANOPROST", "product_id": "64980-516_c9d37a89-f385-4cd5-9a18-15abc5ba2dd9", "dosage_form": "SOLUTION", "product_ndc": "64980-516", "generic_name": "latanoprost", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LATANOPROST", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "ANDA202442", "marketing_category": "ANDA", "marketing_start_date": "20160901", "listing_expiration_date": "20261231"}