prochlorperazine

Generic: prochlorperazine

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

Drug Facts

Product Profile

Brand Name prochlorperazine
Generic Name prochlorperazine
Labeler cosette pharmaceuticals, inc.
Dosage Form SUPPOSITORY
Routes
RECTAL
Active Ingredients

prochlorperazine 25 mg/1

Manufacturer
Cosette Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 0713-0135
Product ID 0713-0135_462a6c34-db6d-8d31-e063-6294a90ae196
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040058
Listing Expiration 2026-12-31
Marketing Start 1993-11-30

Pharmacologic Class

Established (EPC)
phenothiazine [epc]
Chemical Structure
phenothiazines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 07130135
Hyphenated Format 0713-0135

Supplemental Identifiers

RxCUI
198159
UNII
YHP6YLT61T
NUI
N0000175746 M0016525

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 (source: ndc)
Generic Name prochlorperazine (source: ndc)
Application Number ANDA040058 (source: ndc)
Routes
RECTAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1000 BLISTER PACK in 1 CARTON (0713-0135-10) / 1 SUPPOSITORY in 1 BLISTER PACK
  • 12 BLISTER PACK in 1 CARTON (0713-0135-12) / 1 SUPPOSITORY in 1 BLISTER PACK
source: ndc

Packages (2)

0713-0135-10 1000 BLISTER PACK in 1 CARTON (0713-0135-10) / 1 SUPPOSITORY in 1 BLISTER PACK 0713-0135-12 12 BLISTER PACK in 1 CARTON (0713-0135-12) / 1 SUPPOSITORY in 1 BLISTER PACK

Ingredients (1)

prochlorperazine (25 mg/1)

Linked Drug Pages (1)

Prochlorperazine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RECTAL"], "spl_id": "462a6c34-db6d-8d31-e063-6294a90ae196", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["YHP6YLT61T"], "rxcui": ["198159"], "spl_set_id": ["9595346e-76e5-e155-341b-ffaaafb885ab"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Cosette Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 BLISTER PACK in 1 CARTON (0713-0135-10)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "0713-0135-10", "marketing_start_date": "19931130"}, {"sample": false, "description": "12 BLISTER PACK in 1 CARTON (0713-0135-12)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "0713-0135-12", "marketing_start_date": "19931130"}], "brand_name": "Prochlorperazine", "product_id": "0713-0135_462a6c34-db6d-8d31-e063-6294a90ae196", "dosage_form": "SUPPOSITORY", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0713-0135", "generic_name": "Prochlorperazine", "labeler_name": "Cosette Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prochlorperazine", "active_ingredients": [{"name": "PROCHLORPERAZINE", "strength": "25 mg/1"}], "application_number": "ANDA040058", "marketing_category": "ANDA", "marketing_start_date": "19931130", "listing_expiration_date": "20261231"}