timolol hemihydrate
Generic: timolol hemihydrate
Labeler: somerset therapeutics, llcDrug Facts
Product Profile
Brand Name
timolol hemihydrate
Generic Name
timolol hemihydrate
Labeler
somerset therapeutics, llc
Dosage Form
SOLUTION/ DROPS
Routes
Active Ingredients
timolol anhydrous 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70069-698
Product ID
70069-698_c1213979-d6ff-44c2-ad97-1de99ddcf8d2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216654
Listing Expiration
2026-12-31
Marketing Start
2024-10-31
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70069698
Hyphenated Format
70069-698
Supplemental Identifiers
RxCUI
UPC
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
timolol hemihydrate (source: ndc)
Generic Name
timolol hemihydrate (source: ndc)
Application Number
ANDA216654 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (70069-698-01) / 15 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "c1213979-d6ff-44c2-ad97-1de99ddcf8d2", "openfda": {"nui": ["N0000000161", "N0000175556"], "upc": ["0370069697016", "0370069698013", "0370069696019"], "unii": ["5JKY92S7BR"], "rxcui": ["2702393"], "spl_set_id": ["cebc9a5e-0bdb-4f23-9b2c-cde543b62fb6"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70069-698-01) / 15 mL in 1 BOTTLE", "package_ndc": "70069-698-01", "marketing_start_date": "20241031"}], "brand_name": "Timolol Hemihydrate", "product_id": "70069-698_c1213979-d6ff-44c2-ad97-1de99ddcf8d2", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70069-698", "generic_name": "Timolol Hemihydrate", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Timolol Hemihydrate", "active_ingredients": [{"name": "TIMOLOL ANHYDROUS", "strength": "5 mg/mL"}], "application_number": "ANDA216654", "marketing_category": "ANDA", "marketing_start_date": "20241031", "listing_expiration_date": "20261231"}