prochlorperazine edisylate

Generic: prochlorperazine edisylate

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prochlorperazine edisylate
Generic Name prochlorperazine edisylate
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

prochlorperazine edisylate 5 mg/mL

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-523
Product ID 23155-523_d30b8909-61fc-4d53-9a53-0f8612bc2754
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204147
Listing Expiration 2026-12-31
Marketing Start 2015-06-26

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155523
Hyphenated Format 23155-523

Supplemental Identifiers

RxCUI
2102949
UPC
0323155523317
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 ANDA204147 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 PACKAGE (23155-523-41) / 2 mL in 1 VIAL (23155-523-31)
  • 25 VIAL in 1 PACKAGE (23155-523-42) / 2 mL in 1 VIAL (23155-523-31)
source: ndc

Packages (2)

23155-523-41 10 VIAL in 1 PACKAGE (23155-523-41) / 2 mL in 1 VIAL (23155-523-31) 23155-523-42 25 VIAL in 1 PACKAGE (23155-523-42) / 2 mL in 1 VIAL (23155-523-31)

Ingredients (1)

prochlorperazine edisylate (5 mg/mL)

Linked Drug Pages (1)

Prochlorperazine Edisylate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "d30b8909-61fc-4d53-9a53-0f8612bc2754", "openfda": {"upc": ["0323155523317"], "unii": ["PG20W5VQZS"], "rxcui": ["2102949"], "spl_set_id": ["0338b221-db43-45c9-a829-d970fe6643ab"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 PACKAGE (23155-523-41)  / 2 mL in 1 VIAL (23155-523-31)", "package_ndc": "23155-523-41", "marketing_start_date": "20150626"}, {"sample": false, "description": "25 VIAL in 1 PACKAGE (23155-523-42)  / 2 mL in 1 VIAL (23155-523-31)", "package_ndc": "23155-523-42", "marketing_start_date": "20150626"}], "brand_name": "Prochlorperazine Edisylate", "product_id": "23155-523_d30b8909-61fc-4d53-9a53-0f8612bc2754", "dosage_form": "INJECTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "23155-523", "generic_name": "Prochlorperazine Edisylate", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Edisylate", "active_ingredients": [{"name": "PROCHLORPERAZINE EDISYLATE", "strength": "5 mg/mL"}], "application_number": "ANDA204147", "marketing_category": "ANDA", "marketing_start_date": "20150626", "listing_expiration_date": "20261231"}