aripiprazole

Generic: aripiprazole

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

Drug Facts

Product Profile

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

aripiprazole 5 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-820
Product ID 31722-820_10628de5-d649-12ef-e063-6394a90ae380
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205064
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 31722820
Hyphenated Format 31722-820

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UPC
0331722828055 0331722820301
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
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (31722-820-01)
  • 500 TABLET in 1 BOTTLE (31722-820-05)
  • 30 TABLET in 1 BOTTLE (31722-820-30)
  • 10 TABLET in 1 BLISTER PACK (31722-820-31)
  • 250 TABLET in 1 CARTON (31722-820-32)
source: ndc

Packages (5)

31722-820-01 100 TABLET in 1 BOTTLE (31722-820-01) 31722-820-05 500 TABLET in 1 BOTTLE (31722-820-05) 31722-820-30 30 TABLET in 1 BOTTLE (31722-820-30) 31722-820-31 10 TABLET in 1 BLISTER PACK (31722-820-31) 31722-820-32 250 TABLET in 1 CARTON (31722-820-32)

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": "10628de5-d649-12ef-e063-6394a90ae380", "openfda": {"nui": ["N0000175430"], "upc": ["0331722828055", "0331722820301"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["2d8d574b-fbf4-4d2c-a37c-25556ecbf1aa"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-820-01)", "package_ndc": "31722-820-01", "marketing_start_date": "20150428"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-820-05)", "package_ndc": "31722-820-05", "marketing_start_date": "20240202"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (31722-820-30)", "package_ndc": "31722-820-30", "marketing_start_date": "20150428"}, {"sample": false, "description": "10 TABLET in 1 BLISTER PACK (31722-820-31)", "package_ndc": "31722-820-31", "marketing_start_date": "20150428"}, {"sample": false, "description": "250 TABLET in 1 CARTON (31722-820-32)", "package_ndc": "31722-820-32", "marketing_start_date": "20150428"}], "brand_name": "Aripiprazole", "product_id": "31722-820_10628de5-d649-12ef-e063-6394a90ae380", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "31722-820", "generic_name": "Aripiprazole", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA205064", "marketing_category": "ANDA", "marketing_start_date": "20150428", "listing_expiration_date": "20261231"}