NDC 68462-209

Moexipril Hydrochloride

Moexipril Hydrochloride

Moexipril Hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., Usa. The primary component is Moexipril Hydrochloride.

• Product ID: 68462-209_83e29d4f-9c22-42f7-931c-5fcb6bfe21a3
• NDC: 68462-209
• Product Type: Human Prescription Drug
• Proprietary Name: Moexipril Hydrochloride
• Generic Name: Moexipril Hydrochloride
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2010-12-31
• Marketing Category: ANDA / ANDA
• Application Number: ANDA090416
• Labeler Name: Glenmark Pharmaceuticals Inc., USA
• Substance Name: MOEXIPRIL HYDROCHLORIDE
• Active Ingredient Strength: 8 mg/1
• Pharm Classes: Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 68462-209-01

100 TABLET, FILM COATED in 1 BOTTLE (68462-209-01)

• Marketing Start Date: 2010-12-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68462-209-90 [68462020990]

Moexipril Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090416
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-12-31

NDC 68462-209-10 [68462020910]

Moexipril Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090416
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2010-12-31

NDC 68462-209-01 [68462020901]

Moexipril Hydrochloride TABLET, FILM COATED

• Marketing Category: ANDA
• Application Number: ANDA090416
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2010-12-31

Drug Details

Active Ingredients

Ingredient	Strength
MOEXIPRIL HYDROCHLORIDE	7.5 mg/1

OpenFDA Data

• SPL SET ID: baac91ad-f8ee-4694-89f8-5c47a8eda39a
• Manufacturer:
  • Glenmark Pharmaceuticals Inc., USA
• UNII:
  • Q1UMG3UH45
• RxNorm Concept Unique ID - RxCUI:
  • 1299897
  • 1299896

Pharmacological Class

• Angiotensin Converting Enzyme Inhibitor [EPC]
• Angiotensin-converting Enzyme Inhibitors [MoA]
• Angiotensin Converting Enzyme Inhibitor [EPC]
• Angiotensin-converting Enzyme Inhibitors [MoA]

Medicade Reported Pricing

68462020901 MOEXIPRIL HCL 7.5 MG TABLET

Pricing Unit: EA | Drug Type:

NDC Crossover Matching brand name "Moexipril Hydrochloride" or generic name "Moexipril Hydrochloride"

NDC	Brand Name	Generic Name
0093-0017	Moexipril Hydrochloride	Moexipril Hydrochloride
0093-5150	Moexipril Hydrochloride	Moexipril Hydrochloride
68151-1472	Moexipril Hydrochloride	Moexipril Hydrochloride
68151-1473	Moexipril Hydrochloride	Moexipril Hydrochloride
68462-208	Moexipril Hydrochloride	Moexipril Hydrochloride
68462-209	Moexipril Hydrochloride	Moexipril Hydrochloride
0091-3707	Univasc	moexipril hydrochloride