NDC 63629-3390

Benicar

Olmesartan Medoxomil

Benicar is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Olmesartan Medoxomil.

• Product ID: 63629-3390_aa41c784-2ca3-4c6d-8df2-a38714fbadd8
• NDC: 63629-3390
• Product Type: Human Prescription Drug
• Proprietary Name: Benicar
• Generic Name: Olmesartan Medoxomil
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2002-04-25
• Marketing Category: NDA / NDA
• Application Number: NDA021286
• Labeler Name: Bryant Ranch Prepack
• Substance Name: OLMESARTAN MEDOXOMIL
• Active Ingredient Strength: 20 mg/1
• Pharm Classes: Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 63629-3390-1

30 TABLET, FILM COATED in 1 BOTTLE (63629-3390-1)

• Marketing Start Date: 2002-04-25
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 63629-3390-3 [63629339003]

Benicar TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA021286
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-10-12
• Marketing End Date: 2017-10-14

NDC 63629-3390-1 [63629339001]

Benicar TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA021286
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-10-12
• Marketing End Date: 2017-10-14

NDC 63629-3390-2 [63629339002]

Benicar TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA021286
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-10-12
• Marketing End Date: 2017-10-14

NDC 63629-3390-4 [63629339004]

Benicar TABLET, FILM COATED

• Marketing Category: NDA
• Application Number: NDA021286
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2017-10-12
• Marketing End Date: 2017-10-14

Drug Details

Active Ingredients

Ingredient	Strength
OLMESARTAN MEDOXOMIL	20 mg/1

OpenFDA Data

• SPL SET ID: a8f9a538-15db-4bb9-992d-05dc3d9f02c2
• Manufacturer:
  • Bryant Ranch Prepack
• UNII:
  • 6M97XTV3HD
• RxNorm Concept Unique ID - RxCUI:
  • 349401
  • 352200

Pharmacological Class

• Angiotensin 2 Receptor Antagonists [MoA]
• Angiotensin 2 Receptor Blocker [EPC]

NDC Crossover Matching brand name "Benicar" or generic name "Olmesartan Medoxomil"

NDC	Brand Name	Generic Name
0713-0860	Benicar	olmesartan medoxomil
0713-0861	Benicar	olmesartan medoxomil
0713-0862	Benicar	olmesartan medoxomil
68151-4633	Benicar	Benicar
50090-0877	Benicar	Benicar
51138-213	Benicar	Benicar
51138-211	Benicar	Benicar
51138-212	Benicar	Benicar
55289-436	Benicar	Benicar
55154-6130	Benicar	Benicar
63629-3390	Benicar	Benicar
65597-104	Benicar	Benicar
65597-103	Benicar	Benicar
65597-101	Benicar	Benicar
0093-7611	Olmesartan Medoxomil	Olmesartan Medoxomil
0093-7612	Olmesartan Medoxomil	Olmesartan Medoxomil
0378-7012	Olmesartan Medoxomil	olmesartan medoxomil
0378-7112	Olmesartan Medoxomil	olmesartan medoxomil
0378-7124	Olmesartan Medoxomil	olmesartan medoxomil
0527-2425	OLMESARTAN MEDOXOMIL	Olmesartan medoxomil
0527-2426	OLMESARTAN MEDOXOMIL	Olmesartan medoxomil
0527-2427	OLMESARTAN MEDOXOMIL	Olmesartan medoxomil
13668-248	Olmesartan Medoxomil	Olmesartan Medoxomil
13668-249	Olmesartan Medoxomil	Olmesartan Medoxomil
13668-250	Olmesartan Medoxomil	Olmesartan Medoxomil
16729-320	olmesartan medoxomil	olmesartan medoxomil
16729-321	olmesartan medoxomil	olmesartan medoxomil