NDC 0065-0275

Azopt

Brinzolamide

Azopt is a Ophthalmic Suspension/ Drops in the Human Prescription Drug category. It is labeled and distributed by Alcon Laboratories, Inc.. The primary component is Brinzolamide.

• Product ID: 0065-0275_9fb70eb0-176e-432e-8edc-0c1a94bc8ad0
• NDC: 0065-0275
• Product Type: Human Prescription Drug
• Proprietary Name: Azopt
• Generic Name: Brinzolamide
• Dosage Form: Suspension/ Drops
• Route of Administration: OPHTHALMIC
• Marketing Start Date: 1998-04-30
• Marketing Category: NDA / NDA
• Application Number: NDA020816
• Labeler Name: Alcon Laboratories, Inc.
• Substance Name: BRINZOLAMIDE
• Active Ingredient Strength: 10 mg/mL
• Pharm Classes: Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 0065-0275-10

1 BOTTLE, PLASTIC in 1 CARTON (0065-0275-10) > 10 mL in 1 BOTTLE, PLASTIC

• Marketing Start Date: 1998-04-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0065-0275-10 [00065027510]

Azopt SUSPENSION/ DROPS

• Marketing Category: NDA
• Application Number: NDA020816
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 1998-04-30

NDC 0065-0275-15 [00065027515]

Azopt SUSPENSION/ DROPS

• Marketing Category: NDA
• Application Number: NDA020816
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 1998-04-30

NDC 0065-0275-25 [00065027525]

Azopt SUSPENSION/ DROPS

• Marketing Category: NDA
• Application Number: NDA020816
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1998-04-30

NDC 0065-0275-05 [00065027505]

Azopt SUSPENSION/ DROPS

• Marketing Category: NDA
• Application Number: NDA020816
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1998-04-30
• Marketing End Date: 2012-03-12

Drug Details

Active Ingredients

Ingredient	Strength
BRINZOLAMIDE	10 mg/mL

OpenFDA Data

• SPL SET ID: e9ea2ae7-1b98-4034-9fba-8ce2225e0145
• Manufacturer:
  • Alcon Laboratories, Inc.
• UNII:
  • 9451Z89515
• RxNorm Concept Unique ID - RxCUI:
  • 213272
  • 308805

Pharmacological Class

• Carbonic Anhydrase Inhibitor [EPC]
• Carbonic Anhydrase Inhibitors [MoA]

NDC Crossover Matching brand name "Azopt" or generic name "Brinzolamide"

NDC	Brand Name	Generic Name
0065-0275	Azopt	brinzolamide
0078-0722	Azopt	brinzolamide
0591-2127	Brinzolamide	Brinzolamide
0781-6014	Brinzolamide	Brinzolamide
24208-464	BRINZOLAMIDE	brinzolamide
63629-8793	Brinzolamide	Brinzolamide
68682-464	BRINZOLAMIDE	brinzolamide