NDC 78670-100

Corgard

Nadolol

Corgard is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Uswm, Llc. The primary component is Nadolol.

• Product ID: 78670-100_0581ffba-1535-47b5-b8b8-00570be4ef71
• NDC: 78670-100
• Product Type: Human Prescription Drug
• Proprietary Name: Corgard
• Generic Name: Nadolol
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2021-11-18
• Marketing Category: NDA /
• Application Number: NDA018063
• Labeler Name: USWM, LLC
• Substance Name: NADOLOL
• Active Ingredient Strength: 20 mg/1
• Pharm Classes: Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 78670-100-01

100 TABLET in 1 BOTTLE (78670-100-01)

• Marketing Start Date: 2021-11-18
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Corgard" or generic name "Nadolol"

NDC	Brand Name	Generic Name
27505-102	Corgard	Corgard
27505-100	Corgard	Corgard
27505-101	Corgard	Corgard
0093-4235	Nadolol	Nadolol
0093-4236	Nadolol	Nadolol
0093-4237	Nadolol	Nadolol
0378-0028	Nadolol	nadolol
0378-1132	Nadolol	nadolol
0378-1171	Nadolol	nadolol
0781-1181	Nadolol	Nadolol
0781-1182	Nadolol	Nadolol
0781-1183	Nadolol	Nadolol
0781-8004	Nadolol	Nadolol
0781-8005	Nadolol	Nadolol
0781-8006	Nadolol	Nadolol
0904-7070	Nadolol	Nadolol
0904-7071	Nadolol	Nadolol
10135-686	Nadolol	Nadolol
10135-687	Nadolol	Nadolol
10135-688	Nadolol	Nadolol
21695-799	Nadolol	Nadolol
21695-800	Nadolol	Nadolol
21695-802	Nadolol	Nadolol
23155-730	Nadolol	Nadolol
23155-731	Nadolol	Nadolol
23155-732	Nadolol	Nadolol