aripiprazole

Generic: aripiprazole

Labeler: torrent pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler torrent pharmaceuticals limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 2 mg/1

Manufacturer
Torrent Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 13668-216
Product ID 13668-216_264dc32a-9f5f-43be-96ee-0d30503de683
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201519
Listing Expiration 2026-12-31
Marketing Start 2015-04-28

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 13668216
Hyphenated Format 13668-216

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UPC
0313668218305 0313668216301 0313668221305 0313668219302 0313668217308 0313668220308
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 ANDA201519 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (13668-216-01)
  • 500 TABLET in 1 BOTTLE (13668-216-05)
  • 30 TABLET in 1 BOTTLE (13668-216-30)
  • 6250 TABLET in 1 BOTTLE (13668-216-69)
  • 90 TABLET in 1 BOTTLE (13668-216-90)
source: ndc

Packages (5)

13668-216-01 100 TABLET in 1 BOTTLE (13668-216-01) 13668-216-05 500 TABLET in 1 BOTTLE (13668-216-05) 13668-216-30 30 TABLET in 1 BOTTLE (13668-216-30) 13668-216-69 6250 TABLET in 1 BOTTLE (13668-216-69) 13668-216-90 90 TABLET in 1 BOTTLE (13668-216-90)

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": "264dc32a-9f5f-43be-96ee-0d30503de683", "openfda": {"nui": ["N0000175430"], "upc": ["0313668218305", "0313668216301", "0313668221305", "0313668219302", "0313668217308", "0313668220308"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["3988e66f-339c-451e-9f8a-9d0c0a2a381b"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13668-216-01)", "package_ndc": "13668-216-01", "marketing_start_date": "20150428"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13668-216-05)", "package_ndc": "13668-216-05", "marketing_start_date": "20150428"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13668-216-30)", "package_ndc": "13668-216-30", "marketing_start_date": "20150428"}, {"sample": false, "description": "6250 TABLET in 1 BOTTLE (13668-216-69)", "package_ndc": "13668-216-69", "marketing_start_date": "20150428"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (13668-216-90)", "package_ndc": "13668-216-90", "marketing_start_date": "20150428"}], "brand_name": "aripiprazole", "product_id": "13668-216_264dc32a-9f5f-43be-96ee-0d30503de683", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "13668-216", "generic_name": "aripiprazole", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA201519", "marketing_category": "ANDA", "marketing_start_date": "20150428", "listing_expiration_date": "20261231"}