aripiprazole

Generic: aripiprazole

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

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 5 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-7749
Product ID 68788-7749_66441958-c5c0-48a4-850d-bfee07ecff4b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206174
Listing Expiration 2027-12-31
Marketing Start 2020-07-01

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887749
Hyphenated Format 68788-7749

Supplemental Identifiers

RxCUI
402131
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 ANDA206174 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-7749-1)
  • 20 TABLET in 1 BOTTLE (68788-7749-2)
  • 30 TABLET in 1 BOTTLE (68788-7749-3)
  • 60 TABLET in 1 BOTTLE (68788-7749-6)
  • 90 TABLET in 1 BOTTLE (68788-7749-9)
source: ndc

Packages (5)

68788-7749-1 100 TABLET in 1 BOTTLE (68788-7749-1) 68788-7749-2 20 TABLET in 1 BOTTLE (68788-7749-2) 68788-7749-3 30 TABLET in 1 BOTTLE (68788-7749-3) 68788-7749-6 60 TABLET in 1 BOTTLE (68788-7749-6) 68788-7749-9 90 TABLET in 1 BOTTLE (68788-7749-9)

Ingredients (1)

aripiprazole (5 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": "66441958-c5c0-48a4-850d-bfee07ecff4b", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["36fb0c13-dfae-46ac-bb71-0b53fe5649f4"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7749-1)", "package_ndc": "68788-7749-1", "marketing_start_date": "20200701"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68788-7749-2)", "package_ndc": "68788-7749-2", "marketing_start_date": "20200701"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7749-3)", "package_ndc": "68788-7749-3", "marketing_start_date": "20200701"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7749-6)", "package_ndc": "68788-7749-6", "marketing_start_date": "20200701"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7749-9)", "package_ndc": "68788-7749-9", "marketing_start_date": "20200701"}], "brand_name": "Aripiprazole", "product_id": "68788-7749_66441958-c5c0-48a4-850d-bfee07ecff4b", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68788-7749", "generic_name": "Aripiprazole", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA206174", "marketing_category": "ANDA", "marketing_start_date": "20200701", "listing_expiration_date": "20271231"}