latisse

Generic: bimatoprost

Labeler: allergan, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name latisse
Generic Name bimatoprost
Labeler allergan, inc.
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

bimatoprost .3 mg/mL

Manufacturer
Allergan, Inc.

Identifiers & Regulatory

Product NDC 0023-3616
Product ID 0023-3616_f3f30669-e9b1-406b-b6fc-30c520f8ffb3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022369
Listing Expiration 2026-12-31
Marketing Start 2009-01-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00233616
Hyphenated Format 0023-3616

Supplemental Identifiers

RxCUI
1041495 1041497
UNII
QXS94885MZ
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 latisse (source: ndc)
Generic Name bimatoprost (source: ndc)
Application Number NDA022369 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • .3 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, DROPPER in 1 CARTON (0023-3616-05) / 5 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (0023-3616-70) / 3 mL in 1 BOTTLE, DROPPER
  • 1 BOTTLE, DROPPER in 1 CARTON (0023-3616-71) / 3 mL in 1 BOTTLE, DROPPER
source: ndc

Packages (3)

Ingredients (1)

bimatoprost (.3 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "f3f30669-e9b1-406b-b6fc-30c520f8ffb3", "openfda": {"nui": ["N0000175454", "M0017805"], "unii": ["QXS94885MZ"], "rxcui": ["1041495", "1041497"], "spl_set_id": ["34f83d9d-2c64-463e-8a90-9a460fedfead"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-3616-05)  / 5 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-3616-05", "marketing_start_date": "20090126"}, {"sample": false, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-3616-70)  / 3 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-3616-70", "marketing_start_date": "20090126"}, {"sample": true, "description": "1 BOTTLE, DROPPER in 1 CARTON (0023-3616-71)  / 3 mL in 1 BOTTLE, DROPPER", "package_ndc": "0023-3616-71", "marketing_start_date": "20090126"}], "brand_name": "LATISSE", "product_id": "0023-3616_f3f30669-e9b1-406b-b6fc-30c520f8ffb3", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Prostaglandin Analog [EPC]", "Prostaglandins [CS]"], "product_ndc": "0023-3616", "generic_name": "bimatoprost", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LATISSE", "active_ingredients": [{"name": "BIMATOPROST", "strength": ".3 mg/mL"}], "application_number": "NDA022369", "marketing_category": "NDA", "marketing_start_date": "20090126", "listing_expiration_date": "20261231"}