prochlorperazine edisylate

Generic: prochlorperazine edisylate

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

Drug Facts

Product Profile

Brand Name prochlorperazine edisylate
Generic Name prochlorperazine edisylate
Labeler civica, inc.
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

prochlorperazine edisylate 5 mg/mL

Manufacturer
Civica, Inc.

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
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72572580
Hyphenated Format 72572-580

Supplemental Identifiers

RxCUI
314192
UNII
PG20W5VQZS

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (72572-580-25) / 2 mL in 1 VIAL (72572-580-01)
source: ndc

Packages (1)

Ingredients (1)

prochlorperazine edisylate (5 mg/mL)

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"}