NDC 68071-3113

LISINOPRIL

Lisinopril

LISINOPRIL is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Nucare Pharmaceuticals, Inc.. The primary component is Lisinopril.

• Product ID: 68071-3113_4aa40d43-772f-25db-e054-00144ff8d46c
• NDC: 68071-3113
• Product Type: Human Prescription Drug
• Proprietary Name: LISINOPRIL
• Generic Name: Lisinopril
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2016-04-25
• Marketing Category: ANDA / ANDA
• Application Number: ANDA202554
• Labeler Name: NuCare Pharmaceuticals, Inc.
• Substance Name: LISINOPRIL
• Active Ingredient Strength: 10 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 68071-3113-9

90 TABLET in 1 BOTTLE (68071-3113-9)

• Marketing Start Date: 2017-03-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68071-3113-9 [68071311309]

LISINOPRIL TABLET

• Marketing Category: ANDA
• Application Number: ANDA202554
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-03-13
• Marketing End Date: 2019-12-31

NDC 68071-3113-3 [68071311303]

LISINOPRIL TABLET

• Marketing Category: ANDA
• Application Number: ANDA202554
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-03-13
• Marketing End Date: 2019-12-31

NDC 68071-3113-5 [68071311305]

LISINOPRIL TABLET

• Marketing Category: ANDA
• Application Number: ANDA202554
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-03-13
• Marketing End Date: 2019-12-31

NDC 68071-3113-6 [68071311306]

LISINOPRIL TABLET

• Marketing Category: ANDA
• Application Number: ANDA202554
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2017-03-13
• Marketing End Date: 2019-12-31

Drug Details

Active Ingredients

Ingredient	Strength
LISINOPRIL	10 mg/1

OpenFDA Data

• SPL SET ID: 4aa40d43-772e-25db-e054-00144ff8d46c
• Manufacturer:
  • NuCare Pharmaceuticals, Inc.
• UNII:
  • E7199S1YWR
• RxNorm Concept Unique ID - RxCUI:
  • 314076

Pharmacological Class

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

NDC Crossover Matching brand name "LISINOPRIL" or generic name "Lisinopril"

NDC	Brand Name	Generic Name
0143-1266	Lisinopril	Lisinopril
0143-1267	Lisinopril	Lisinopril
0143-1268	Lisinopril	Lisinopril
0143-1270	Lisinopril	Lisinopril
0143-9713	Lisinopril	Lisinopril
0143-9714	Lisinopril	Lisinopril
0143-9715	Lisinopril	Lisinopril
0185-0025	lisinopril	lisinopril
0185-0101	lisinopril	lisinopril
0185-0102	lisinopril	lisinopril
0185-0103	lisinopril	lisinopril
0185-0104	lisinopril	lisinopril
0185-0602	lisinopril	lisinopril
0185-0605	lisinopril	lisinopril
0185-0610	lisinopril	lisinopril
0185-0620	lisinopril	lisinopril
0185-0630	lisinopril	lisinopril
0185-0640	lisinopril	lisinopril
0185-5400	lisinopril	lisinopril
0378-2072	Lisinopril	lisinopril
0378-2073	Lisinopril	lisinopril
0378-2074	Lisinopril	lisinopril
0378-2075	Lisinopril	lisinopril
0378-2076	Lisinopril	lisinopril
68001-270	lisinopril	lisinopril
68001-271	lisinopril	lisinopril
68001-267	lisinopril	lisinopril
68001-272	lisinopril	lisinopril
68001-334	Lisinopril	Lisinopril
68001-268	lisinopril	lisinopril
68001-333	Lisinopril	Lisinopril
68001-335	Lisinopril	Lisinopril
68001-337	Lisinopril	Lisinopril
68001-269	lisinopril	lisinopril
68001-336	Lisinopril	Lisinopril
68001-332	Lisinopril	Lisinopril
68071-1672	LISINOPRIL	LISINOPRIL
68071-1775	LISINOPRIL	LISINOPRIL
68071-3064	LISINOPRIL	LISINOPRIL
68071-1894	LISINOPRIL	LISINOPRIL
68071-3220	LISINOPRIL	LISINOPRIL
68071-3113	LISINOPRIL	LISINOPRIL
68071-3122	LISINOPRIL	LISINOPRIL
68071-1931	Lisinopril	Lisinopril
68071-3070	lisinopril	lisinopril
68071-3043	LISINOPRIL	LISINOPRIL
68071-3123	LISINOPRIL	LISINOPRIL
68071-3145	LISINOPRIL	LISINOPRIL
68071-3178	LISINOPRIL	LISINOPRIL
68071-4660	Lisinopril	Lisinopril