tafluprost
Generic: tafluprost
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
tafluprost
Generic Name
tafluprost
Labeler
sandoz inc
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
tafluprost .0045 mg/.3mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-6184
Product ID
0781-6184_bfffa484-4105-45ec-ab1d-124e96639f35
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209040
Listing Expiration
2026-12-31
Marketing Start
2022-12-05
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07816184
Hyphenated Format
0781-6184
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
tafluprost (source: ndc)
Generic Name
tafluprost (source: ndc)
Application Number
ANDA209040 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .0045 mg/.3mL
Packaging
- 6 POUCH in 1 CARTON (0781-6184-87) / 5 CONTAINER in 1 POUCH (0781-6184-14) / .3 mL in 1 CONTAINER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "bfffa484-4105-45ec-ab1d-124e96639f35", "openfda": {"nui": ["N0000175454", "N0000000106", "N0000009526", "M0017805"], "unii": ["1O6WQ6T7G3"], "rxcui": ["1244611"], "spl_set_id": ["bfffa484-4105-45ec-ab1d-124e96639f35"], "pharm_class_cs": ["Prostaglandins [CS]"], "pharm_class_pe": ["Increased Prostaglandin Activity [PE]"], "pharm_class_epc": ["Prostaglandin Analog [EPC]"], "pharm_class_moa": ["Prostaglandin Receptor Agonists [MoA]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POUCH in 1 CARTON (0781-6184-87) / 5 CONTAINER in 1 POUCH (0781-6184-14) / .3 mL in 1 CONTAINER", "package_ndc": "0781-6184-87", "marketing_start_date": "20221205"}], "brand_name": "Tafluprost", "product_id": "0781-6184_bfffa484-4105-45ec-ab1d-124e96639f35", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Increased Prostaglandin Activity [PE]", "Prostaglandin Analog [EPC]", "Prostaglandin Receptor Agonists [MoA]", "Prostaglandins [CS]"], "product_ndc": "0781-6184", "generic_name": "Tafluprost", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tafluprost", "active_ingredients": [{"name": "TAFLUPROST", "strength": ".0045 mg/.3mL"}], "application_number": "ANDA209040", "marketing_category": "ANDA", "marketing_start_date": "20221205", "listing_expiration_date": "20261231"}