felodipine

Generic: felodipine

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

Drug Facts

Product Profile

Brand Name felodipine
Generic Name felodipine
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

felodipine 5 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-921
Product ID 71205-921_06c9bc5a-7a0f-483d-bd5c-61768db340bb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204800
Listing Expiration 2026-12-31
Marketing Start 2020-10-12

Pharmacologic Class

Established (EPC)
dihydropyridine calcium channel blocker [epc]
Mechanism of Action
calcium channel antagonists [moa]
Chemical Structure
dihydropyridines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205921
Hyphenated Format 71205-921

Supplemental Identifiers

RxCUI
402695 402696 402698
UPC
0371205920302
UNII
OL961R6O2C
NUI
N0000000069 N0000175421 M0006414

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 felodipine (source: ndc)
Generic Name felodipine (source: ndc)
Application Number ANDA204800 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (71205-921-00)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-921-30)
  • 500 TABLET, FILM COATED in 1 BOTTLE (71205-921-55)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-921-60)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71205-921-72)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-921-90)
source: ndc

Packages (6)

71205-921-00 100 TABLET, FILM COATED in 1 BOTTLE (71205-921-00) 71205-921-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-921-30) 71205-921-55 500 TABLET, FILM COATED in 1 BOTTLE (71205-921-55) 71205-921-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-921-60) 71205-921-72 120 TABLET, FILM COATED in 1 BOTTLE (71205-921-72) 71205-921-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-921-90)

Ingredients (1)

felodipine (5 mg/1)

Linked Drug Pages (1)

Felodipine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "06c9bc5a-7a0f-483d-bd5c-61768db340bb", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0371205920302"], "unii": ["OL961R6O2C"], "rxcui": ["402695", "402696", "402698"], "spl_set_id": ["2c4dd9a4-61ca-4c88-90f6-12d9e0fdb7cd"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71205-921-00)", "package_ndc": "71205-921-00", "marketing_start_date": "20210618"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-921-30)", "package_ndc": "71205-921-30", "marketing_start_date": "20210618"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71205-921-55)", "package_ndc": "71205-921-55", "marketing_start_date": "20210618"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-921-60)", "package_ndc": "71205-921-60", "marketing_start_date": "20210618"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71205-921-72)", "package_ndc": "71205-921-72", "marketing_start_date": "20210618"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-921-90)", "package_ndc": "71205-921-90", "marketing_start_date": "20210618"}], "brand_name": "Felodipine", "product_id": "71205-921_06c9bc5a-7a0f-483d-bd5c-61768db340bb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "71205-921", "generic_name": "Felodipine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felodipine", "active_ingredients": [{"name": "FELODIPINE", "strength": "5 mg/1"}], "application_number": "ANDA204800", "marketing_category": "ANDA", "marketing_start_date": "20201012", "listing_expiration_date": "20261231"}