latanoprost

Generic: latanoprost

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name latanoprost
Generic Name latanoprost
Labeler nucare pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
OPHTHALMIC
Active Ingredients

latanoprost 50 ug/mL

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3884
Product ID 68071-3884_3c477d33-a8ca-d39f-e063-6294a90ac5f0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091449
Listing Expiration 2026-12-31
Marketing Start 2011-01-07

Pharmacologic Class

Established (EPC)
prostaglandin analog [epc]
Chemical Structure
prostaglandins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713884
Hyphenated Format 68071-3884

Supplemental Identifiers

RxCUI
314072
UPC
0368071388428
UNII
6Z5B6HVF6O
NUI
N0000175454 M0017805

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 ANDA091449 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 50 ug/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (68071-3884-2) / 2.5 mL in 1 BOTTLE
source: ndc

Packages (1)

68071-3884-2 1 BOTTLE in 1 CARTON (68071-3884-2) / 2.5 mL in 1 BOTTLE

Ingredients (1)

latanoprost (50 ug/mL)

Linked Drug Pages (1)

Latanoprost ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "3c477d33-a8ca-d39f-e063-6294a90ac5f0", "openfda": {"nui": ["N0000175454", "M0017805"], "upc": ["0368071388428"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["3c47a089-2c72-f58c-e063-6294a90a4cce"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68071-3884-2)  / 2.5 mL in 1 BOTTLE", "package_ndc": "68071-3884-2", "marketing_start_date": "20250813"}], "brand_name": "Latanoprost", "product_id": "68071-3884_3c477d33-a8ca-d39f-e063-6294a90ac5f0", "dosage_form": "SOLUTION", "product_ndc": "68071-3884", "generic_name": "Latanoprost", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Latanoprost", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "ANDA091449", "marketing_category": "ANDA", "marketing_start_date": "20110107", "listing_expiration_date": "20261231"}