perphenazine
Generic: perphenazine
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
perphenazine
Generic Name
perphenazine
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
perphenazine 8 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-1133
Product ID
70518-1133_485af52b-093a-0570-e063-6294a90a1b42
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205973
Listing Expiration
2027-12-31
Marketing Start
2018-04-24
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705181133
Hyphenated Format
70518-1133
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
perphenazine (source: ndc)
Generic Name
perphenazine (source: ndc)
Application Number
ANDA205973 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1133-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "485af52b-093a-0570-e063-6294a90a1b42", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198078"], "spl_set_id": ["8028ab47-a6de-4924-a4cd-9336fa90dd90"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1133-0)", "package_ndc": "70518-1133-0", "marketing_start_date": "20180424"}], "brand_name": "Perphenazine", "product_id": "70518-1133_485af52b-093a-0570-e063-6294a90a1b42", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-1133", "generic_name": "Perphenazine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "8 mg/1"}], "application_number": "ANDA205973", "marketing_category": "ANDA", "marketing_start_date": "20180424", "listing_expiration_date": "20271231"}