amlodipine besylate

Generic: amlodipine besylate

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

Drug Facts

Product Profile

Brand Name amlodipine besylate
Generic Name amlodipine besylate
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amlodipine besylate 10 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6808
Product ID 50090-6808_01a4a136-ecab-4c98-a853-c5750e70605b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203245
Listing Expiration 2026-12-31
Marketing Start 2019-05-22

Pharmacologic Class

Classes
calcium channel antagonists [moa] calcium channel blocker [epc] cytochrome p450 3a inhibitors [moa] dihydropyridine calcium channel blocker [epc] dihydropyridines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500906808
Hyphenated Format 50090-6808

Supplemental Identifiers

RxCUI
308135
UNII
864V2Q084H

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 amlodipine besylate (source: ndc)
Generic Name amlodipine besylate (source: ndc)
Application Number ANDA203245 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6808-0)
  • 90 TABLET in 1 BOTTLE (50090-6808-1)
  • 100 TABLET in 1 BOTTLE (50090-6808-2)
source: ndc

Packages (3)

50090-6808-0 30 TABLET in 1 BOTTLE (50090-6808-0) 50090-6808-1 90 TABLET in 1 BOTTLE (50090-6808-1) 50090-6808-2 100 TABLET in 1 BOTTLE (50090-6808-2)

Ingredients (1)

amlodipine besylate (10 mg/1)

Linked Drug Pages (1)

Amlodipine Besylate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "01a4a136-ecab-4c98-a853-c5750e70605b", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["5c50c3fe-afe5-459e-95c0-c9af4cbb6909"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6808-0)", "package_ndc": "50090-6808-0", "marketing_start_date": "20231107"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6808-1)", "package_ndc": "50090-6808-1", "marketing_start_date": "20231107"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6808-2)", "package_ndc": "50090-6808-2", "marketing_start_date": "20231107"}], "brand_name": "Amlodipine Besylate", "product_id": "50090-6808_01a4a136-ecab-4c98-a853-c5750e70605b", "dosage_form": "TABLET", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "50090-6808", "generic_name": "Amlodipine Besylate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}], "application_number": "ANDA203245", "marketing_category": "ANDA", "marketing_start_date": "20190522", "listing_expiration_date": "20261231"}