protopam chloride

Generic: pralidoxime chloride

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name protopam chloride
Generic Name pralidoxime chloride
Labeler baxter healthcare corporation
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

pralidoxime chloride 1 g/20mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 60977-141
Product ID 60977-141_6227f4ba-9aa6-4344-a5a7-e45789669627
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA014134
Listing Expiration 2026-12-31
Marketing Start 1965-03-10

Pharmacologic Class

Classes
cholinesterase reactivator [epc] cholinesterase reactivators [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60977141
Hyphenated Format 60977-141

Supplemental Identifiers

RxCUI
208969 312576
UNII
38X7XS076H

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 protopam chloride (source: ndc)
Generic Name pralidoxime chloride (source: ndc)
Application Number NDA014134 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/20mL
source: ndc
Packaging
  • 6 VIAL, SINGLE-DOSE in 1 PACKAGE (60977-141-01) / 20 mL in 1 VIAL, SINGLE-DOSE (60977-141-27)
source: ndc

Packages (1)

60977-141-01 6 VIAL, SINGLE-DOSE in 1 PACKAGE (60977-141-01) / 20 mL in 1 VIAL, SINGLE-DOSE (60977-141-27)

Ingredients (1)

pralidoxime chloride (1 g/20mL)

Linked Drug Pages (1)

Protopam Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "6227f4ba-9aa6-4344-a5a7-e45789669627", "openfda": {"unii": ["38X7XS076H"], "rxcui": ["208969", "312576"], "spl_set_id": ["2741d8fd-51c2-46be-880b-99f2b20a6137"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 VIAL, SINGLE-DOSE in 1 PACKAGE (60977-141-01)  / 20 mL in 1 VIAL, SINGLE-DOSE (60977-141-27)", "package_ndc": "60977-141-01", "marketing_start_date": "19650310"}], "brand_name": "Protopam Chloride", "product_id": "60977-141_6227f4ba-9aa6-4344-a5a7-e45789669627", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Cholinesterase Reactivator [EPC]", "Cholinesterase Reactivators [MoA]"], "product_ndc": "60977-141", "generic_name": "pralidoxime chloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Protopam Chloride", "active_ingredients": [{"name": "PRALIDOXIME CHLORIDE", "strength": "1 g/20mL"}], "application_number": "NDA014134", "marketing_category": "NDA", "marketing_start_date": "19650310", "listing_expiration_date": "20261231"}