latisse
Generic: bimatoprost
Labeler: allergan, inc.Drug Facts
Product Profile
Brand Name
latisse
Generic Name
bimatoprost
Labeler
allergan, inc.
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
bimatoprost .3 mg/mL
Manufacturer
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)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00233616
Hyphenated Format
0023-3616
Supplemental Identifiers
RxCUI
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
latisse (source: ndc)
Generic Name
bimatoprost (source: ndc)
Application Number
NDA022369 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .3 mg/mL
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
Packages (3)
Ingredients (1)
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"}