aripiprazole

Generic: aripiprazole

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 15 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1935
Product ID 71335-1935_565dd1b2-149c-4475-abac-65d6aa107f94
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207105
Listing Expiration 2027-12-31
Marketing Start 2019-02-27

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351935
Hyphenated Format 71335-1935

Supplemental Identifiers

RxCUI
349490
UNII
82VFR53I78
NUI
N0000175430

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 aripiprazole (source: ndc)
Generic Name aripiprazole (source: ndc)
Application Number ANDA207105 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1935-1)
  • 15 TABLET in 1 BOTTLE (71335-1935-2)
  • 28 TABLET in 1 BOTTLE (71335-1935-3)
  • 60 TABLET in 1 BOTTLE (71335-1935-4)
  • 90 TABLET in 1 BOTTLE (71335-1935-5)
  • 120 TABLET in 1 BOTTLE (71335-1935-6)
source: ndc

Packages (6)

71335-1935-1 30 TABLET in 1 BOTTLE (71335-1935-1) 71335-1935-2 15 TABLET in 1 BOTTLE (71335-1935-2) 71335-1935-3 28 TABLET in 1 BOTTLE (71335-1935-3) 71335-1935-4 60 TABLET in 1 BOTTLE (71335-1935-4) 71335-1935-5 90 TABLET in 1 BOTTLE (71335-1935-5) 71335-1935-6 120 TABLET in 1 BOTTLE (71335-1935-6)

Ingredients (1)

aripiprazole (15 mg/1)

Linked Drug Pages (1)

Aripiprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "565dd1b2-149c-4475-abac-65d6aa107f94", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349490"], "spl_set_id": ["1ef9e44f-5672-47c2-97e9-286e1b84417d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1935-1)", "package_ndc": "71335-1935-1", "marketing_start_date": "20210824"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-1935-2)", "package_ndc": "71335-1935-2", "marketing_start_date": "20240408"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1935-3)", "package_ndc": "71335-1935-3", "marketing_start_date": "20240408"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1935-4)", "package_ndc": "71335-1935-4", "marketing_start_date": "20240408"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1935-5)", "package_ndc": "71335-1935-5", "marketing_start_date": "20220127"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1935-6)", "package_ndc": "71335-1935-6", "marketing_start_date": "20240408"}], "brand_name": "Aripiprazole", "product_id": "71335-1935_565dd1b2-149c-4475-abac-65d6aa107f94", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "71335-1935", "generic_name": "Aripiprazole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "15 mg/1"}], "application_number": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20190227", "listing_expiration_date": "20271231"}