amlodipine besylate 10 mg

Generic: amlodipine besylate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name amlodipine besylate 10 mg
Generic Name amlodipine besylate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

amlodipine besylate 10 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8451
Product ID 68788-8451_57f51242-eb35-4bb6-8a3b-3d0f43b1966e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078414
Listing Expiration 2027-12-31
Marketing Start 2023-05-30

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 687888451
Hyphenated Format 68788-8451

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 10 mg (source: ndc)
Generic Name amlodipine besylate (source: ndc)
Application Number ANDA078414 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-8451-1)
  • 30 TABLET in 1 BOTTLE (68788-8451-3)
  • 60 TABLET in 1 BOTTLE (68788-8451-6)
  • 90 TABLET in 1 BOTTLE (68788-8451-9)
source: ndc

Packages (4)

68788-8451-1 100 TABLET in 1 BOTTLE (68788-8451-1) 68788-8451-3 30 TABLET in 1 BOTTLE (68788-8451-3) 68788-8451-6 60 TABLET in 1 BOTTLE (68788-8451-6) 68788-8451-9 90 TABLET in 1 BOTTLE (68788-8451-9)

Ingredients (1)

amlodipine besylate (10 mg/1)

Linked Drug Pages (1)

AMLODIPINE BESYLATE 10 mg ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "57f51242-eb35-4bb6-8a3b-3d0f43b1966e", "openfda": {"unii": ["864V2Q084H"], "rxcui": ["308135"], "spl_set_id": ["ea9f44a1-96cf-496a-8c07-18d8de27e512"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8451-1)", "package_ndc": "68788-8451-1", "marketing_start_date": "20230530"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8451-3)", "package_ndc": "68788-8451-3", "marketing_start_date": "20230530"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8451-6)", "package_ndc": "68788-8451-6", "marketing_start_date": "20230530"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8451-9)", "package_ndc": "68788-8451-9", "marketing_start_date": "20230530"}], "brand_name": "AMLODIPINE BESYLATE 10 mg", "product_id": "68788-8451_57f51242-eb35-4bb6-8a3b-3d0f43b1966e", "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": "68788-8451", "generic_name": "AMLODIPINE BESYLATE", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMLODIPINE BESYLATE", "brand_name_suffix": "10 mg", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}], "application_number": "ANDA078414", "marketing_category": "ANDA", "marketing_start_date": "20230530", "listing_expiration_date": "20271231"}