flecainide acetate

Generic: flecainide acetate tablet

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flecainide acetate
Generic Name flecainide acetate tablet
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

flecainide acetate 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-155
Product ID 82804-155_ee590951-cce8-4a1e-b3bd-ae0b610ebda9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075882
Listing Expiration 2026-12-31
Marketing Start 2015-12-28

Pharmacologic Class

Classes
antiarrhythmic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804155
Hyphenated Format 82804-155

Supplemental Identifiers

RxCUI
886662
UPC
0382804155309
UNII
M8U465Q1WQ

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 flecainide acetate (source: ndc)
Generic Name flecainide acetate tablet (source: ndc)
Application Number ANDA075882 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (82804-155-30)
source: ndc

Packages (1)

Ingredients (1)

flecainide acetate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee590951-cce8-4a1e-b3bd-ae0b610ebda9", "openfda": {"upc": ["0382804155309"], "unii": ["M8U465Q1WQ"], "rxcui": ["886662"], "spl_set_id": ["ee590951-cce8-4a1e-b3bd-ae0b610ebda9"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-155-30)", "package_ndc": "82804-155-30", "marketing_start_date": "20241003"}], "brand_name": "Flecainide Acetate", "product_id": "82804-155_ee590951-cce8-4a1e-b3bd-ae0b610ebda9", "dosage_form": "TABLET", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "82804-155", "generic_name": "Flecainide Acetate Tablet", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flecainide Acetate", "active_ingredients": [{"name": "FLECAINIDE ACETATE", "strength": "50 mg/1"}], "application_number": "ANDA075882", "marketing_category": "ANDA", "marketing_start_date": "20151228", "listing_expiration_date": "20261231"}