aripiprazole

Generic: aripiprazole

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name aripiprazole
Generic Name aripiprazole
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

aripiprazole 5 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-2150
Product ID 70518-2150_49d9bcfb-fe1e-d5b5-e063-6294a90ac4ab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202101
Listing Expiration 2027-12-31
Marketing Start 2019-06-24

Pharmacologic Class

Established (EPC)
atypical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705182150
Hyphenated Format 70518-2150

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 ANDA202101 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-2150-2)
source: ndc

Packages (1)

70518-2150-2 30 TABLET in 1 BLISTER PACK (70518-2150-2)

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": "49d9bcfb-fe1e-d5b5-e063-6294a90ac4ab", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["99747897-22fe-4bee-9942-6349c0c8f6b0"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2150-2)", "package_ndc": "70518-2150-2", "marketing_start_date": "20250708"}], "brand_name": "Aripiprazole", "product_id": "70518-2150_49d9bcfb-fe1e-d5b5-e063-6294a90ac4ab", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2150", "generic_name": "Aripiprazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA202101", "marketing_category": "ANDA", "marketing_start_date": "20190624", "listing_expiration_date": "20271231"}