bimatoprost

Generic: bimatoprost

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

Drug Facts

Product Profile

Brand Name bimatoprost
Generic Name bimatoprost
Labeler sandoz inc
Dosage Form SOLUTION/ DROPS
Routes
OPHTHALMIC
Active Ingredients

bimatoprost .3 mg/mL

Manufacturer
Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-6206
Product ID 0781-6206_68075f38-ba3d-4a73-b51a-b1b70177067d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202719
Listing Expiration 2026-12-31
Marketing Start 2016-12-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07816206
Hyphenated Format 0781-6206

Supplemental Identifiers

RxCUI
1041495
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 bimatoprost (source: ndc)
Generic Name bimatoprost (source: ndc)
Application Number ANDA202719 (source: ndc)
Routes
OPHTHALMIC
source: ndc

Resolved Composition

Strengths
  • .3 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-75) / 5 mL in 1 BOTTLE, WITH APPLICATOR
  • 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-93) / 3 mL in 1 BOTTLE, WITH APPLICATOR
source: ndc

Packages (2)

0781-6206-75 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-75) / 5 mL in 1 BOTTLE, WITH APPLICATOR 0781-6206-93 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-93) / 3 mL in 1 BOTTLE, WITH APPLICATOR

Ingredients (1)

bimatoprost (.3 mg/mL)

Linked Drug Pages (1)

Bimatoprost ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "68075f38-ba3d-4a73-b51a-b1b70177067d", "openfda": {"nui": ["N0000175454", "M0017805"], "unii": ["QXS94885MZ"], "rxcui": ["1041495"], "spl_set_id": ["27bef7e1-750a-4ac1-ab5f-e4c0121ffcbc"], "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, WITH APPLICATOR in 1 CARTON (0781-6206-75)  / 5 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "0781-6206-75", "marketing_start_date": "20161206"}, {"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (0781-6206-93)  / 3 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "0781-6206-93", "marketing_start_date": "20161206"}], "brand_name": "Bimatoprost", "product_id": "0781-6206_68075f38-ba3d-4a73-b51a-b1b70177067d", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Prostaglandin Analog [EPC]", "Prostaglandins [CS]"], "product_ndc": "0781-6206", "generic_name": "Bimatoprost", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bimatoprost", "active_ingredients": [{"name": "BIMATOPROST", "strength": ".3 mg/mL"}], "application_number": "ANDA202719", "marketing_category": "ANDA", "marketing_start_date": "20161206", "listing_expiration_date": "20261231"}