felodipine

Generic: felodipine

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name felodipine
Generic Name felodipine
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

felodipine 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-5870
Product ID 50090-5870_4c349c25-c277-4c0f-9ca4-f5296b652eff
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203417
Listing Expiration 2026-12-31
Marketing Start 2013-01-17

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 500905870
Hyphenated Format 50090-5870

Supplemental Identifiers

RxCUI
402695
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 ANDA203417 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5870-0)
source: ndc

Packages (1)

50090-5870-0 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5870-0)

Ingredients (1)

felodipine (10 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": "4c349c25-c277-4c0f-9ca4-f5296b652eff", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["OL961R6O2C"], "rxcui": ["402695"], "spl_set_id": ["be3bc927-1ba5-4cdd-9986-64ff29789d7e"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5870-0)", "package_ndc": "50090-5870-0", "marketing_start_date": "20211209"}], "brand_name": "Felodipine", "product_id": "50090-5870_4c349c25-c277-4c0f-9ca4-f5296b652eff", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "50090-5870", "generic_name": "Felodipine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felodipine", "active_ingredients": [{"name": "FELODIPINE", "strength": "10 mg/1"}], "application_number": "ANDA203417", "marketing_category": "ANDA", "marketing_start_date": "20130117", "listing_expiration_date": "20261231"}