latanoprost

Generic: latanoprost

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name latanoprost
Generic Name latanoprost
Labeler somerset therapeutics, llc
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

latanoprost 50 ug/mL

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-421
Product ID 70069-421_836e9c6e-15a0-41bd-b3bb-bd864a5fd1bd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201786
Listing Expiration 2027-12-31
Marketing Start 2019-12-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069421
Hyphenated Format 70069-421

Supplemental Identifiers

RxCUI
314072
UPC
0370069421017 0370069421031
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 ANDA201786 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • 50 ug/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (70069-421-01) / 2.5 mL in 1 BOTTLE
  • 3 BOTTLE in 1 CARTON (70069-421-03) / 2.5 mL in 1 BOTTLE
source: ndc

Packages (2)

70069-421-01 1 BOTTLE in 1 CARTON (70069-421-01) / 2.5 mL in 1 BOTTLE 70069-421-03 3 BOTTLE in 1 CARTON (70069-421-03) / 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": "836e9c6e-15a0-41bd-b3bb-bd864a5fd1bd", "openfda": {"nui": ["N0000175454", "M0017805"], "upc": ["0370069421017", "0370069421031"], "unii": ["6Z5B6HVF6O"], "rxcui": ["314072"], "spl_set_id": ["5d0b99ad-f05a-44c7-ac61-26b5a533ea8d"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70069-421-01)  / 2.5 mL in 1 BOTTLE", "package_ndc": "70069-421-01", "marketing_start_date": "20191203"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (70069-421-03)  / 2.5 mL in 1 BOTTLE", "package_ndc": "70069-421-03", "marketing_start_date": "20191203"}], "brand_name": "LATANOPROST", "product_id": "70069-421_836e9c6e-15a0-41bd-b3bb-bd864a5fd1bd", "dosage_form": "SOLUTION/ DROPS", "product_ndc": "70069-421", "generic_name": "LATANOPROST", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LATANOPROST", "active_ingredients": [{"name": "LATANOPROST", "strength": "50 ug/mL"}], "application_number": "ANDA201786", "marketing_category": "ANDA", "marketing_start_date": "20191203", "listing_expiration_date": "20271231"}