NDC 10191-1177

CHLORALUM

Chloral Hydrate

CHLORALUM is a Sublingual Pellet in the Human Prescription Drug category. It is labeled and distributed by Remedy Makers. The primary component is Chloral Hydrate.

• Product ID: 10191-1177_67f493a4-72e1-4c84-8230-ac298d890d12
• NDC: 10191-1177
• Product Type: Human Prescription Drug
• Proprietary Name: CHLORALUM
• Generic Name: Chloral Hydrate
• Dosage Form: Pellet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 2000-02-04
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Remedy Makers
• Substance Name: CHLORAL HYDRATE
• Active Ingredient Strength: 3 [hp_X]/1
• DEA Schedule: CIV
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10191-1177-2

172 PELLET in 1 VIAL, GLASS (10191-1177-2)

• Marketing Start Date: 2000-02-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10191-1177-2 [10191117702]

CHLORALUM PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2000-02-04
• Inactivation Date: 2019-10-29

Drug Details

Active Ingredients

Ingredient	Strength
CHLORAL HYDRATE	3 [hp_X]/1

OpenFDA Data

• SPL SET ID: 2978bcfb-5d29-434e-b973-501360972b2e
• Manufacturer:
  • Remedy Makers
• UNII:
  • 418M5916WG
• UPC Code:
  • 0310191117723

NDC Crossover Matching brand name "CHLORALUM" or generic name "Chloral Hydrate"

NDC	Brand Name	Generic Name
0220-6462	Chloralum	CHLORAL HYDRATE
10191-1177	CHLORALUM	CHLORAL HYDRATE