aripiprazole
Generic: aripiprazole
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
aripiprazole
Generic Name
aripiprazole
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
aripiprazole 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-2897
Product ID
70518-2897_4ab86cb8-ceac-1e02-e063-6394a90a17e6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207105
Listing Expiration
2027-12-31
Marketing Start
2020-09-28
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705182897
Hyphenated Format
70518-2897
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA207105 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 TABLET in 1 BLISTER PACK (70518-2897-0)
- 30 TABLET in 1 BOTTLE, PLASTIC (70518-2897-1)
- 180 TABLET in 1 BOTTLE, PLASTIC (70518-2897-2)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ab86cb8-ceac-1e02-e063-6394a90a17e6", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["433cdc7d-465a-4ad4-bd84-cabd37e15f51"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2897-0)", "package_ndc": "70518-2897-0", "marketing_start_date": "20200928"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-2897-1)", "package_ndc": "70518-2897-1", "marketing_start_date": "20250701"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-2897-2)", "package_ndc": "70518-2897-2", "marketing_start_date": "20251016"}], "brand_name": "Aripiprazole", "product_id": "70518-2897_4ab86cb8-ceac-1e02-e063-6394a90a17e6", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2897", "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": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20200928", "listing_expiration_date": "20271231"}