NDC 44911-0171

Salmonella

Salmonella Typhi

Salmonella is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Energique, Inc.. The primary component is Salmonella Enterica Subsp. Enterica Serovar Typhi.

• Product ID: 44911-0171_2ec9dcf3-c13e-48b5-9223-e947bc8ab9bc
• NDC: 44911-0171
• Product Type: Human Otc Drug
• Proprietary Name: Salmonella
• Generic Name: Salmonella Typhi
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-06-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Energique, Inc.
• Substance Name: SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI
• Active Ingredient Strength: 200 [hp_C]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 44911-0171-1

30 mL in 1 BOTTLE, DROPPER (44911-0171-1)

• Marketing Start Date: 2015-06-17
• Marketing End Date: 2022-06-18
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 44911-0171-1 [44911017101]

Salmonella LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-06-17
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI	200 [hp_C]/mL

OpenFDA Data

• SPL SET ID: e5d3f863-4fda-4a91-97fa-95f939372585
• Manufacturer:
  • Energique, Inc.
• UNII:
  • 760T5R8B3O

NDC Crossover Matching brand name "Salmonella" or generic name "Salmonella Typhi"

NDC	Brand Name	Generic Name
44911-0171	Salmonella	Salmonella Typhi
57520-0362	Salmonella	Salmonella