latanoprost
Generic: latanoprost
Labeler: glenmark pharmaceuticals incDrug Facts
Product Profile
Brand Name
latanoprost
Generic Name
latanoprost
Labeler
glenmark pharmaceuticals inc
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
latanoprost 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68462-944
Product ID
68462-944_ff864618-ca49-4dd2-8e7f-1b14477c3a15
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218257
Listing Expiration
2026-12-31
Marketing Start
2024-11-26
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68462944
Hyphenated Format
68462-944
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
ANDA218257 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 1 BOTTLE in 1 CARTON (68462-944-03) / 2.5 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "ff864618-ca49-4dd2-8e7f-1b14477c3a15", "openfda": {"nui": ["N0000175454", "M0017805"], "upc": ["0368462944035"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["821d2ad5-a430-4fd2-8cfd-50b2118b8639"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["GLENMARK PHARMACEUTICALS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68462-944-03) / 2.5 mL in 1 BOTTLE", "package_ndc": "68462-944-03", "marketing_start_date": "20241126"}], "brand_name": "latanoprost", "product_id": "68462-944_ff864618-ca49-4dd2-8e7f-1b14477c3a15", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "68462-944", "generic_name": "latanoprost", "labeler_name": "GLENMARK PHARMACEUTICALS INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "latanoprost", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "ANDA218257", "marketing_category": "ANDA", "marketing_start_date": "20241126", "listing_expiration_date": "20261231"}