lisinopril

Generic: lisinopril

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

lisinopril 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-786
Product ID 43063-786_32850517-fae5-3e53-e063-6294a90adf73
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076164
Listing Expiration 2026-12-31
Marketing Start 2011-11-01

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 43063786
Hyphenated Format 43063-786

Supplemental Identifiers

RxCUI
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 ANDA076164 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 14 TABLET in 1 BOTTLE, PLASTIC (43063-786-14)
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-786-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (43063-786-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-786-90)
  • 180 TABLET in 1 BOTTLE, PLASTIC (43063-786-93)
  • 120 TABLET in 1 BOTTLE, PLASTIC (43063-786-98)
source: ndc

Packages (6)

Ingredients (1)

lisinopril (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32850517-fae5-3e53-e063-6294a90adf73", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["e4c11545-00da-4675-856a-7e600a2f4bd9"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (43063-786-14)", "package_ndc": "43063-786-14", "marketing_start_date": "20170831"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-786-30)", "package_ndc": "43063-786-30", "marketing_start_date": "20170831"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-786-60)", "package_ndc": "43063-786-60", "marketing_start_date": "20170920"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-786-90)", "package_ndc": "43063-786-90", "marketing_start_date": "20170831"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (43063-786-93)", "package_ndc": "43063-786-93", "marketing_start_date": "20170928"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE, PLASTIC (43063-786-98)", "package_ndc": "43063-786-98", "marketing_start_date": "20171003"}], "brand_name": "LISINOPRIL", "product_id": "43063-786_32850517-fae5-3e53-e063-6294a90adf73", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "43063-786", "generic_name": "Lisinopril", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}