felodipine

Generic: felodipine extended-release tablets

Labeler: yiling pharmaceutical inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name felodipine
Generic Name felodipine extended-release tablets
Labeler yiling pharmaceutical inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

felodipine 5 mg/1

Manufacturer
Yiling Pharmaceutical Inc.

Identifiers & Regulatory

Product NDC 69117-0029
Product ID 69117-0029_47236bb3-7d75-0c2a-e063-6394a90a7ac7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210847
Listing Expiration 2026-12-31
Marketing Start 2019-08-01

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 691170029
Hyphenated Format 69117-0029

Supplemental Identifiers

RxCUI
402695 402696 402698
UPC
0369117003022 0369117003015 0369117002827 0369117002919 0369117002810 0369117002926
UNII
OL961R6O2C
NUI
N0000000069 N0000175421 M0006414

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 felodipine (source: ndc)
Generic Name felodipine extended-release tablets (source: ndc)
Application Number ANDA210847 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0029-1)
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0029-2)
source: ndc

Packages (2)

69117-0029-1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0029-1) 69117-0029-2 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0029-2)

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": "47236bb3-7d75-0c2a-e063-6394a90a7ac7", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0369117003022", "0369117003015", "0369117002827", "0369117002919", "0369117002810", "0369117002926"], "unii": ["OL961R6O2C"], "rxcui": ["402695", "402696", "402698"], "spl_set_id": ["7990a581-3e0f-5d8c-e053-2991aa0aa6a7"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Yiling Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0029-1)", "package_ndc": "69117-0029-1", "marketing_start_date": "20190801"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69117-0029-2)", "package_ndc": "69117-0029-2", "marketing_start_date": "20190801"}], "brand_name": "Felodipine", "product_id": "69117-0029_47236bb3-7d75-0c2a-e063-6394a90a7ac7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "69117-0029", "generic_name": "Felodipine Extended-release Tablets", "labeler_name": "Yiling Pharmaceutical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Felodipine", "active_ingredients": [{"name": "FELODIPINE", "strength": "5 mg/1"}], "application_number": "ANDA210847", "marketing_category": "ANDA", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}