← Current compounder rows

Current NDC auxiliary source row compounder:618

This page is keyed by dataset, FDA.report source record ID, and physical source row number. Empty values are shown rather than omitted.

Complete normalized row#

Record Source
ndc_compounder_zip
Product Ndc Raw
83863-7536
Product Ndc
83863-7536
Product Ndc Digits
838637536
Product Type Name
HUMAN COMPOUNDED DRUG
Proprietary Name
Succinylcholine Chloride 100 mg in 5 mL (20 mg/mL)
Proprietary Name Suffix
[empty]
Nonproprietary Name
Succinylcholine Chloride 100 mg in 5 mL (20 mg/mL)
Dosage Form Name
INJECTION
Route Name
INTRAVENOUS
Marketing Category Name
OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name
Park Avenue Compounding
Establishment Name
Park Avenue Compounding
Establishment Fei
[empty]
Substance Name
SUCCINYLCHOLINE CHLORIDE
Active Ingredients Info
20 mg/1 mL
History Active Ingredients Raw
SUCCINYLCHOLINE CHLORIDE
History Active Ingredients Info Raw
20 mg/1 mL
History Dosage Raw
INJECTION
Dea Schedule
[empty]
Package Ndc Raw
83863-7536-1
Package Ndc
83863-7536-1
Package Ndc Digits
8386375361
Package Ndc11
83863753601
Package Description
5 mL in 1 SYRINGE, PLASTIC (83863-7536-1)
Reporting Period Raw
2026-1
Reporting Period
2026-1
Normalization Status
valid
Source Url
https://www.accessdata.fda.gov/cder/compounders_ndc_directory.zip
Source Archive
compounders_ndc_directory.zip
Source File
compounders_ndc_directory.txt
Source Date
2026-09-18
Source Last Modified
Fri, 18 Sep 2026 15:17:23 GMT
Source Archive Sha256
222f6800f79cb1a0fa79431b7226bd6b34899999dbf086af51004a96774ada98
Source Member Sha256
f8d9743e5616579a34d614887e86a53913efa0a63d3138d59d2f87cbb4d0cc17
Source Record Id
compounder:618
Source Row Number
618
Source Row Hash
c0b753c4d8373bee88e020abc1624a401c0b5a8065ae533f703b5e9f538a1ddf
Import Run Id
20261015T162751Z
Loaded At
2026-10-15 16:32:20

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "83863-7536",
    "DEASCHEDULE": "",
    "LABELERNAME": "Park Avenue Compounding",
    "SUBSTANCENAME": "SUCCINYLCHOLINE CHLORIDE",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "83863-7536-1",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Succinylcholine Chloride 100 mg in 5 mL (20 mg/mL)",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "Succinylcholine Chloride 100 mg in 5 mL (20 mg/mL)",
    "PACKAGEDESCRIPTION": "5 mL in 1 SYRINGE, PLASTIC (83863-7536-1) ",
    "ACTIVEINGREDIENTSINFO": "20 mg/1 mL",
    "MARKETINGCATEGORYNAME": "OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)",
    "PROPRIETARYNAMESUFFIX": ""
}

Normalization notes#

[]

Current status projection#

Dataset
compounder
Record Source
ndc_compounder_zip
Source Record Id
compounder:618
Source Row Number
618
Status Scope
package
Lookup Ndc
83863-7536-1
Lookup Ndc Digits
8386375361
Product Ndc
83863-7536
Product Ndc Digits
838637536
Package Ndc
83863-7536-1
Package Ndc Digits
8386375361
Package Ndc11
83863753601
Product Id
[empty]
Status Code
COMPOUNDER
Status Label
Outsourcing facility compounded drug report
Reporting Period Raw
2026-1
Reporting Period
2026-1
Source Table
fda_ndc_aux_compounder
Source File
compounders_ndc_directory.txt
Source Date
2026-09-18
Source Row Hash
c0b753c4d8373bee88e020abc1624a401c0b5a8065ae533f703b5e9f538a1ddf
Import Run Id
20261015T162751Z
Loaded At
2026-10-15 16:32:20