norvasc

Generic: amlodipine besylate

Labeler: pfizer laboratories div pfizer inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name norvasc
Generic Name amlodipine besylate
Labeler pfizer laboratories div pfizer inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amlodipine besylate 5 mg/1

Manufacturer
PFIZER LABORATORIES DIV PFIZER INC

Identifiers & Regulatory

Product NDC 0069-1530
Product ID 0069-1530_3714a872-b6c6-4d74-88d2-add8a895e311
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019787
Marketing Start 1992-07-31
Marketing End 2027-07-31

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 00691530
Hyphenated Format 0069-1530

Supplemental Identifiers

RxCUI
197361 212542 212549 212575 308135 308136
UNII
864V2Q084H

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 norvasc (source: ndc)
Generic Name amlodipine besylate (source: ndc)
Application Number NDA019787 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (0069-1530-68)
  • 300 TABLET in 1 BOTTLE (0069-1530-72)
source: ndc

Packages (2)

0069-1530-68 90 TABLET in 1 BOTTLE (0069-1530-68) 0069-1530-72 300 TABLET in 1 BOTTLE (0069-1530-72)

Ingredients (1)

amlodipine besylate (5 mg/1)

Linked Drug Pages (1)

Norvasc ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3714a872-b6c6-4d74-88d2-add8a895e311", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361", "212542", "212549", "212575", "308135", "308136"], "spl_set_id": ["abd6a2ca-40c2-485c-bc53-db1c652505ed"], "manufacturer_name": ["PFIZER LABORATORIES DIV PFIZER INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (0069-1530-68)", "package_ndc": "0069-1530-68", "marketing_end_date": "20270731", "marketing_start_date": "19920731"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (0069-1530-72)", "package_ndc": "0069-1530-72", "marketing_end_date": "20260930", "marketing_start_date": "19920731"}], "brand_name": "Norvasc", "product_id": "0069-1530_3714a872-b6c6-4d74-88d2-add8a895e311", "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": "0069-1530", "generic_name": "amlodipine besylate", "labeler_name": "PFIZER LABORATORIES DIV PFIZER INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Norvasc", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}], "application_number": "NDA019787", "marketing_category": "NDA", "marketing_end_date": "20270731", "marketing_start_date": "19920731"}