aripiprazole

Generic: aripiprazole

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler northstar rxllc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 2 mg/1

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 16714-141
Product ID 16714-141_04230bfc-e6ad-1844-e063-6394a90a939e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205064
Listing Expiration 2026-12-31
Marketing Start 2020-10-01

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 16714141
Hyphenated Format 16714-141

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UNII
82VFR53I78
NUI
N0000175430

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 aripiprazole (source: ndc)
Generic Name aripiprazole (source: ndc)
Application Number ANDA205064 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (16714-141-01)
source: ndc

Packages (1)

16714-141-01 30 TABLET in 1 BOTTLE (16714-141-01)

Ingredients (1)

aripiprazole (2 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": "04230bfc-e6ad-1844-e063-6394a90a939e", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["f87dbfe4-5417-47c9-a97f-d246cfc10023"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (16714-141-01)", "package_ndc": "16714-141-01", "marketing_start_date": "20201001"}], "brand_name": "Aripiprazole", "product_id": "16714-141_04230bfc-e6ad-1844-e063-6394a90a939e", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "16714-141", "generic_name": "Aripiprazole", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA205064", "marketing_category": "ANDA", "marketing_start_date": "20201001", "listing_expiration_date": "20261231"}