amlodipine besylate

Generic: amlodipine besylate

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amlodipine besylate
Generic Name amlodipine besylate
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amlodipine besylate 5 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-291
Product ID 51655-291_48e70fe2-0d8d-38de-e063-6294a90a198d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078925
Listing Expiration 2027-12-31
Marketing Start 2022-10-27

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 51655291
Hyphenated Format 51655-291

Supplemental Identifiers

RxCUI
197361
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
  • 5 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (51655-291-26)
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-291-52)
source: ndc

Packages (2)

51655-291-26 90 TABLET in 1 BOTTLE, PLASTIC (51655-291-26) 51655-291-52 30 TABLET in 1 BOTTLE, PLASTIC (51655-291-52)

Ingredients (1)

amlodipine besylate (5 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": "48e70fe2-0d8d-38de-e063-6294a90a198d", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["197361"], "spl_set_id": ["f2b8274b-d849-6793-e053-2a95a90aa0e8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-291-26)", "package_ndc": "51655-291-26", "marketing_start_date": "20230403"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-291-52)", "package_ndc": "51655-291-52", "marketing_start_date": "20221027"}], "brand_name": "Amlodipine Besylate", "product_id": "51655-291_48e70fe2-0d8d-38de-e063-6294a90a198d", "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": "51655-291", "generic_name": "Amlodipine besylate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine Besylate", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}], "application_number": "ANDA078925", "marketing_category": "ANDA", "marketing_start_date": "20221027", "listing_expiration_date": "20271231"}