prochlorperazine edisylate
Generic: prochlorperazine edisylate
Labeler: fosun pharma usa incDrug Facts
Product Profile
Brand Name
prochlorperazine edisylate
Generic Name
prochlorperazine edisylate
Labeler
fosun pharma usa inc
Dosage Form
INJECTION
Routes
Active Ingredients
prochlorperazine edisylate 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72266-204
Product ID
72266-204_24fdbe72-a9c4-6144-e063-6394a90ac10d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214107
Listing Expiration
2026-12-31
Marketing Start
2023-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72266204
Hyphenated Format
72266-204
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
ANDA214107 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 10 VIAL in 1 CARTON (72266-204-10) / 2 mL in 1 VIAL (72266-204-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "24fdbe72-a9c4-6144-e063-6394a90ac10d", "openfda": {"unii": ["PG20W5VQZS"], "rxcui": ["2102949"], "spl_set_id": ["f793cdb3-9fd8-79e1-e053-6394a90ae08b"], "manufacturer_name": ["FOSUN PHARMA USA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72266-204-10) / 2 mL in 1 VIAL (72266-204-01)", "package_ndc": "72266-204-10", "marketing_start_date": "20230501"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "72266-204_24fdbe72-a9c4-6144-e063-6394a90ac10d", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "72266-204", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "FOSUN PHARMA USA INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Edisylate", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA214107", "marketing_category": "ANDA", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}