felodipine

Generic: felodipine

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name felodipine
Generic Name felodipine
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

felodipine 5 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-049
Product ID 23155-049_c39f92ed-6e77-4742-b4e4-deec031f1e31
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201964
Listing Expiration 2026-12-31
Marketing Start 2013-11-08

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 23155049
Hyphenated Format 23155-049

Supplemental Identifiers

RxCUI
402695 402696 402698
UPC
0323155048018 0323155049015 0323155050011
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 (source: ndc)
Application Number ANDA201964 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-049-01)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-049-05)
source: ndc

Packages (2)

23155-049-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-049-01) 23155-049-05 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-049-05)

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": "c39f92ed-6e77-4742-b4e4-deec031f1e31", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0323155048018", "0323155049015", "0323155050011"], "unii": ["OL961R6O2C"], "rxcui": ["402695", "402696", "402698"], "spl_set_id": ["0bef7cf2-012b-4804-ac93-0a8b333035db"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-049-01)", "package_ndc": "23155-049-01", "marketing_start_date": "20131108"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (23155-049-05)", "package_ndc": "23155-049-05", "marketing_start_date": "20131108"}], "brand_name": "FELODIPINE", "product_id": "23155-049_c39f92ed-6e77-4742-b4e4-deec031f1e31", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "23155-049", "generic_name": "FELODIPINE", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FELODIPINE", "active_ingredients": [{"name": "FELODIPINE", "strength": "5 mg/1"}], "application_number": "ANDA201964", "marketing_category": "ANDA", "marketing_start_date": "20131108", "listing_expiration_date": "20261231"}