prochlorperazine edisylate
Generic: prochlorperazine edisylate
Labeler: civica, inc.Drug Facts
Product Profile
Brand Name
prochlorperazine edisylate
Generic Name
prochlorperazine edisylate
Labeler
civica, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
prochlorperazine edisylate 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72572-580
Product ID
72572-580_7395a535-b3fc-4bb8-b2e1-d8c42b9a0509
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089903
Listing Expiration
2026-12-31
Marketing Start
2019-11-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72572580
Hyphenated Format
72572-580
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
prochlorperazine edisylate (source: ndc)
Generic Name
prochlorperazine edisylate (source: ndc)
Application Number
ANDA089903 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 25 VIAL in 1 CARTON (72572-580-25) / 2 mL in 1 VIAL (72572-580-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "7395a535-b3fc-4bb8-b2e1-d8c42b9a0509", "openfda": {"unii": ["PG20W5VQZS"], "rxcui": ["314192"], "spl_set_id": ["e3e0c6c5-6b92-40e0-a926-29c64846be93"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72572-580-25) / 2 mL in 1 VIAL (72572-580-01)", "package_ndc": "72572-580-25", "marketing_start_date": "20191118"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "72572-580_7395a535-b3fc-4bb8-b2e1-d8c42b9a0509", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72572-580", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Edisylate", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA089903", "marketing_category": "ANDA", "marketing_start_date": "20191118", "listing_expiration_date": "20261231"}