aripiprazole

Generic: aripiprazole

Labeler: dr.reddys laboratories inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler dr.reddys laboratories inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 30 mg/1

Manufacturer
Dr.Reddys Laboratories Inc

Identifiers & Regulatory

Product NDC 43598-970
Product ID 43598-970_5be74c47-c62f-40f5-8aad-bd20f8f4cae3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206383
Listing Expiration 2026-12-31
Marketing Start 2020-03-16

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43598970
Hyphenated Format 43598-970

Supplemental Identifiers

RxCUI
349490 349545 349547 349553 402131 602964
UPC
0343598965307 0343598968308 0343598969305 0343598967301 0343598966304 0343598970301
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 ANDA206383 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 500 TABLET in 1 BOTTLE (43598-970-05)
  • 30 TABLET in 1 BOTTLE (43598-970-30)
source: ndc

Packages (2)

43598-970-05 500 TABLET in 1 BOTTLE (43598-970-05) 43598-970-30 30 TABLET in 1 BOTTLE (43598-970-30)

Ingredients (1)

aripiprazole (30 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": "5be74c47-c62f-40f5-8aad-bd20f8f4cae3", "openfda": {"nui": ["N0000175430"], "upc": ["0343598965307", "0343598968308", "0343598969305", "0343598967301", "0343598966304", "0343598970301"], "unii": ["82VFR53I78"], "rxcui": ["349490", "349545", "349547", "349553", "402131", "602964"], "spl_set_id": ["178f09f0-e08e-452b-b817-717c5c49e110"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Dr.Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (43598-970-05)", "package_ndc": "43598-970-05", "marketing_start_date": "20200316"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (43598-970-30)", "package_ndc": "43598-970-30", "marketing_start_date": "20200316"}], "brand_name": "Aripiprazole", "product_id": "43598-970_5be74c47-c62f-40f5-8aad-bd20f8f4cae3", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "43598-970", "generic_name": "Aripiprazole", "labeler_name": "Dr.Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "30 mg/1"}], "application_number": "ANDA206383", "marketing_category": "ANDA", "marketing_start_date": "20200316", "listing_expiration_date": "20261231"}