lisinopril

Generic: lisinopril

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 5 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-6797
Product ID 0904-6797_5efe4f9d-62f8-4c2e-a8ef-37c1a1ca0b3d
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 09046797
Hyphenated Format 0904-6797

Supplemental Identifiers

RxCUI
197884 311354 314076 314077
UNII
E7199S1YWR

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
  • 5 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-6797-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-6797-61 100 BLISTER PACK in 1 CARTON (0904-6797-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

lisinopril (5 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": "5efe4f9d-62f8-4c2e-a8ef-37c1a1ca0b3d", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["197884", "311354", "314076", "314077"], "spl_set_id": ["faade1f8-f901-40f9-a5a2-2a00e8aa94d1"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6797-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6797-61", "marketing_start_date": "20060113"}], "brand_name": "Lisinopril", "product_id": "0904-6797_5efe4f9d-62f8-4c2e-a8ef-37c1a1ca0b3d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "0904-6797", "generic_name": "Lisinopril", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "5 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20060113", "listing_expiration_date": "20261231"}