prochlorperazine maleate

Generic: prochlorperazine maleate

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

Drug Facts

Product Profile

Brand Name prochlorperazine maleate
Generic Name prochlorperazine maleate
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

prochlorperazine maleate 10 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4200
Product ID 70518-4200_3ff4e764-1554-cca9-e063-6294a90accb7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216495
Listing Expiration 2026-12-31
Marketing Start 2024-10-02

Pharmacologic Class

Classes
phenothiazine [epc] phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184200
Hyphenated Format 70518-4200

Supplemental Identifiers

RxCUI
198365
UNII
I1T8O1JTL6

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 maleate (source: ndc)
Generic Name prochlorperazine maleate (source: ndc)
Application Number ANDA216495 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE, PLASTIC (70518-4200-0)
source: ndc

Packages (1)

70518-4200-0 10 TABLET in 1 BOTTLE, PLASTIC (70518-4200-0)

Ingredients (1)

prochlorperazine maleate (10 mg/1)

Linked Drug Pages (1)

Prochlorperazine Maleate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ff4e764-1554-cca9-e063-6294a90accb7", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365"], "spl_set_id": ["5c1dd0ea-89e9-4317-a83e-5e15da79ca20"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (70518-4200-0)", "package_ndc": "70518-4200-0", "marketing_start_date": "20241002"}], "brand_name": "Prochlorperazine Maleate", "product_id": "70518-4200_3ff4e764-1554-cca9-e063-6294a90accb7", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4200", "generic_name": "Prochlorperazine Maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine Maleate", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA216495", "marketing_category": "ANDA", "marketing_start_date": "20241002", "listing_expiration_date": "20261231"}