amlodipine besylate

Generic: amlodipine besylate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amlodipine besylate
Generic Name amlodipine besylate
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amlodipine besylate 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-041
Product ID 43063-041_41365d1f-a1bc-7f51-e063-6394a90a8766
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078925
Listing Expiration 2026-12-31
Marketing Start 2010-10-20

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 43063041
Hyphenated Format 43063-041

Supplemental Identifiers

RxCUI
308135
UPC
0343063041901
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 ANDA078925 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-041-30)
  • 90 TABLET in 1 BOTTLE, PLASTIC (43063-041-90)
source: ndc

Packages (2)

43063-041-30 30 TABLET in 1 BOTTLE, PLASTIC (43063-041-30) 43063-041-90 90 TABLET in 1 BOTTLE, PLASTIC (43063-041-90)

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": "41365d1f-a1bc-7f51-e063-6394a90a8766", "openfda": {"upc": ["0343063041901"], "unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["47114f60-4151-43d4-ac2d-adc49492a679"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-041-30)", "package_ndc": "43063-041-30", "marketing_start_date": "20130207"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-041-90)", "package_ndc": "43063-041-90", "marketing_start_date": "20130207"}], "brand_name": "Amlodipine Besylate", "product_id": "43063-041_41365d1f-a1bc-7f51-e063-6394a90a8766", "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": "43063-041", "generic_name": "Amlodipine besylate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}], "application_number": "ANDA078925", "marketing_category": "ANDA", "marketing_start_date": "20101020", "listing_expiration_date": "20261231"}