latanoprost

Generic: latanoprost

Labeler: sandoz inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name latanoprost
Generic Name latanoprost
Labeler sandoz inc
Dosage Form SOLUTION
Routes
OPHTHALMIC
Active Ingredients

latanoprost 50 ug/mL

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 61314-547
Product ID 61314-547_a4388e84-6b82-4d7d-915b-6997d4b44b36
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 61314547
Hyphenated Format 61314-547

Supplemental Identifiers

RxCUI
314072
UNII
6Z5B6HVF6O
NUI
N0000175454 M0017805

Packaging Origin

Original Packager
true

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 (61314-547-01) / 2.5 mL in 1 BOTTLE
  • 3 BOTTLE in 1 CARTON (61314-547-03) / 2.5 mL in 1 BOTTLE
source: ndc

Packages (2)

Ingredients (1)

latanoprost (50 ug/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "a4388e84-6b82-4d7d-915b-6997d4b44b36", "openfda": {"nui": ["N0000175454", "M0017805"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["1fba56a6-c8dc-4f34-b05d-efdea75d2fea"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (61314-547-01)  / 2.5 mL in 1 BOTTLE", "package_ndc": "61314-547-01", "marketing_start_date": "20110107"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (61314-547-03)  / 2.5 mL in 1 BOTTLE", "package_ndc": "61314-547-03", "marketing_start_date": "20110107"}], "brand_name": "Latanoprost", "product_id": "61314-547_a4388e84-6b82-4d7d-915b-6997d4b44b36", "dosage_form": "SOLUTION", "product_ndc": "61314-547", "generic_name": "Latanoprost", "labeler_name": "Sandoz 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"}