Betimol is a Ophthalmic Solution/ Drops in the Human Prescription Drug category. It is labeled and distributed by Akorn. The primary component is Timolol.
Product ID | 76478-001_1148d491-87d2-4423-8486-4e5355e968ed |
NDC | 76478-001 |
Product Type | Human Prescription Drug |
Proprietary Name | Betimol |
Generic Name | Timolol |
Dosage Form | Solution/ Drops |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 2014-01-02 |
Marketing Category | NDA / NDA |
Application Number | NDA020439 |
Labeler Name | Akorn |
Substance Name | TIMOLOL |
Active Ingredient Strength | 3 mg/mL |
Pharm Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2014-01-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA020439 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2014-01-02 |
Marketing Category | NDA |
Application Number | NDA020439 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-01-02 |
Marketing Category | NDA |
Application Number | NDA020439 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2014-01-02 |
Ingredient | Strength |
---|---|
TIMOLOL | 2.56 mg/mL |
SPL SET ID: | 3d7acd55-33b1-4a24-99ae-01f87b0dca1f |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
68669-522 | Betimol | timolol |
68669-525 | Betimol | timolol |
76478-001 | Betimol | Timolol |
76478-002 | Betimol | Timolol |
82584-001 | BETIMOL | timolol |
82584-002 | BETIMOL | timolol |
17478-189 | Timolol Maleate | Timolol |
17478-365 | Timolol Maleate | Timolol |
17478-366 | Timolol Maleate | Timolol |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BETIMOL 79128616 4442019 Live/Registered |
Akorn International S.Ã .r.l. 2013-02-15 |
BETIMOL 74628335 1961729 Live/Registered |
AKORN INTERNATIONAL S.A.R.L. 1995-02-01 |