lisinopril

Generic: lisinopril

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler lupin pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 20 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-515
Product ID 68180-515_6723a96d-02f8-40c2-95ec-89a7053a7117
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2026-12-31
Marketing Start 2006-01-13

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180515
Hyphenated Format 68180-515

Supplemental Identifiers

RxCUI
197884 205326 311353 311354 314076 314077
UPC
0368180513018 0368180512028 0368180513032
UNII
E7199S1YWR

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lisinopril (source: ndc)
Generic Name lisinopril (source: ndc)
Application Number ANDA077321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 16 HOW SUPPLIED/STORAGE AND HANDLING Lisinopril tablet USP is available as uncoated biconvex tablets in bottles of below mentioned pack size Strength Color Shape Scored Side 1/Side 2 NDC 2.5 mg White to off-white Round No LUPIN/2.5 Bottles of 100: 68180-512-01 Bottles of 500: 68180-512-02 5 mg Pink Round Yes 5/Breakline Bottles of 100: 68180-513-01 Bottles of 1000: 68180-513-03 10 mg Pink Round No LUPIN/10 Bottles of 100: 68180-980-01 Bottles of 1000: 68180-980-03 20 mg Pink Round No LUPIN/20 Bottles of 100: 68180-981-01 Bottles of 1000: 68180-981-03 30 mg Red Round No LUPIN/30 Bottles of 100: 68180-982-01 Bottles of 500: 68180-982-02 40 mg Yellow Round No LUPIN/40 Bottles of 100: 68180-979-01 Bottles of 1000: 68180-979-03 Store at controlled room temperature, 20° to 25°C (68° to 77°F) [see USP]. Protect from moisture, freezing and excessive heat. Dispense in a tight container.
  • LISINOPRIL TABLETS USP Rx Only 2.5 mg NDC 68180-512-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 2.5 mg NDC 68180-512-02 500 Tablets LISINOPRIL TABLETS USP Rx Only 5 mg NDC 68180-513-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 5 mg NDC 68180-513-03 1000 Tablets LISINOPRIL TABLETS USP Rx Only 10 mg NDC 68180-980-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 10 mg NDC 68180-980-03 1000 Tablets LISINOPRIL TABLETS USP Rx Only 20 mg NDC 68180-981-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 20 mg NDC 68180-981-03 1000 Tablets LISINOPRIL TABLETS USP Rx Only 30 mg NDC 68180-982-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 30 mg NDC 68180-982-02 500 Tablets LISINOPRIL TABLETS USP Rx Only 40 mg NDC 68180-979-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 40 mg NDC 68180-979-03 1000 Tablets LISINOPRIL TABLETS USP Rx Only 2.5 mg NDC 68180-512-01 100 Tablets LISINOPRIL TABLETS USP Rx Only Lisinopril Tablets USP 2.5 mg NDC 68180-512-02 500 Tablets LISINOPRIL TABLETS USP Rx Only 5 mg NDC 68180-513-01 100 Tablets LISINOPRIL TABLETS USP Rx Only Lisinopril Tablets USP 5 mg NDC 68180-513-03 1000 Tablets LISINOPRIL TABLETS USP Rx Only 10 mg NDC 68180-514-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 10 mg NDC 68180-980-03 1000 Tablets LISINOPRIL TABLETS USP Rx Only 20 mg NDC 68180-515-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 20 mg NDC 68180-981-03 1000 Tablets LISINOPRIL TABLETS USP Rx Only 30 mg NDC 68180-516-01 100 Tabl LISINOPRIL TABLETS USP Rx Only 30 mg NDC 68180-982-02 500 Tablets LISINOPRIL TABLETS USP Rx Only 40 mg NDC 68180-979-01 100 Tablets LISINOPRIL TABLETS USP Rx Only 40 mg NDC 68180-979-03 1000 Tablets
source: label

Packages (0)

No package records.

Ingredients (1)

lisinopril (20 mg/1)

Linked Drug Pages (1)

Lisinopril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6723a96d-02f8-40c2-95ec-89a7053a7117", "openfda": {"upc": ["0368180513018", "0368180512028", "0368180513032"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["7d6c31e2-b5a4-4279-8013-a8dad37ea73b"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [], "brand_name": "Lisinopril", "product_id": "68180-515_6723a96d-02f8-40c2-95ec-89a7053a7117", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68180-515", "generic_name": "Lisinopril", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20060113", "listing_expiration_date": "20261231"}