Drugplain

Indigo 100 [hp_C]/1

Indigo · PELLET · Hahnemann Laboratories, INC.

1 Recall on Record
Plain English

Indigo is a pellet containing indigo at 100 [hp_C]/1, taken oral. Manufactured by Hahnemann Laboratories, INC..

Key Facts

Brand Name
Indigo
Generic Name
Indigo
NDC Code (Product)
37662-3691
Manufacturer
Hahnemann Laboratories, INC.
Strength
100 [hp_C]/1
Dosage Form
PELLET
Route
ORAL
Marketing Status
Marketing Start
08/03/2023

Recall History

1 Recall on Record
Class I01/25/2015

Detox Transforms

Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein, making iNDiGO an unapproved drug.

TerminatedVoluntary: Firm initiated

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

anaemia1 reports
aplastic anaemia1 reports
asthenia1 reports
bile duct stenosis1 reports
cholangiocarcinoma1 reports
death1 reports
drug ineffective1 reports
epistaxis1 reports
feeling hot1 reports
hernia1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Frequently Asked Questions

What is Indigo used for?

Indigo contains Indigo. It is a pellet taken oral. Consult your doctor for specific uses.

Is Indigo a controlled substance?

Indigo is not classified as a controlled substance by the DEA.

What is the generic name for Indigo?

The generic name for Indigo is Indigo. There are 2 other brand versions of Indigo.

What is the NDC code for Indigo 100 [hp_C]/1?

The NDC (National Drug Code) for Indigo 100 [hp_C]/1 is 37662-3691, listed by Hahnemann Laboratories, INC..

Product NDC

37662-3691

Package NDC

37662-3691-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)