entacapone

Generic: entacapone

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name entacapone
Generic Name entacapone
Labeler lannett company, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

entacapone 200 mg/1

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-1830
Product ID 0527-1830_071b5720-d208-9e0e-e063-6294a90a0513
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206669
Listing Expiration 2026-12-31
Marketing Start 2018-12-20

Pharmacologic Class

Established (EPC)
catechol-o-methyltransferase inhibitor [epc]
Mechanism of Action
catechol o-methyltransferase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05271830
Hyphenated Format 0527-1830

Supplemental Identifiers

RxCUI
317094
UPC
0305271830371
UNII
4975G9NM6T
NUI
N0000175756 N0000175757

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 entacapone (source: ndc)
Generic Name entacapone (source: ndc)
Application Number ANDA206669 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1830-37)
source: ndc

Packages (1)

0527-1830-37 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1830-37)

Ingredients (1)

entacapone (200 mg/1)

Linked Drug Pages (1)

Entacapone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "071b5720-d208-9e0e-e063-6294a90a0513", "openfda": {"nui": ["N0000175756", "N0000175757"], "upc": ["0305271830371"], "unii": ["4975G9NM6T"], "rxcui": ["317094"], "spl_set_id": ["0bf133e4-1c17-4358-9a43-144e6bf2564f"], "pharm_class_epc": ["Catechol-O-Methyltransferase Inhibitor [EPC]"], "pharm_class_moa": ["Catechol O-Methyltransferase Inhibitors [MoA]"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1830-37)", "package_ndc": "0527-1830-37", "marketing_start_date": "20181220"}], "brand_name": "Entacapone", "product_id": "0527-1830_071b5720-d208-9e0e-e063-6294a90a0513", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Catechol O-Methyltransferase Inhibitors [MoA]", "Catechol-O-Methyltransferase Inhibitor [EPC]"], "product_ndc": "0527-1830", "generic_name": "entacapone", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Entacapone", "active_ingredients": [{"name": "ENTACAPONE", "strength": "200 mg/1"}], "application_number": "ANDA206669", "marketing_category": "ANDA", "marketing_start_date": "20181220", "listing_expiration_date": "20261231"}