NDC 48951-4051

Euphrasia

Euphrasia

Euphrasia is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Euphrasia. The primary component is Euphrasia Stricta.

• Product ID: 48951-4051_6c41ab9f-d451-fc18-e053-2a91aa0ae235
• NDC: 48951-4051
• Product Type: Human Otc Drug
• Proprietary Name: Euphrasia
• Generic Name: Euphrasia
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Euphrasia
• Substance Name: EUPHRASIA STRICTA
• Active Ingredient Strength: 3 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 48951-4051-1

1 BOTTLE, DROPPER in 1 BAG (48951-4051-1) > 7 mL in 1 BOTTLE, DROPPER

• Marketing Start Date: 2009-09-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48951-4051-1 [48951405101]

Euphrasia LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2009-09-01
• Marketing End Date: 2019-09-06

Drug Details

Active Ingredients

Ingredient	Strength
EUPHRASIA STRICTA	3 [hp_X]/mL

OpenFDA Data

• SPL SET ID: b490acbd-e14e-4a76-bfce-97d3962d6377
• Manufacturer:
  • Euphrasia
• UNII:
  • C9642I91WL

NDC Crossover Matching brand name "Euphrasia" or generic name "Euphrasia"

NDC	Brand Name	Generic Name
0360-0171	EUPHRASIA	EUPHRASIA STRICTA
48951-4051	Euphrasia	Euphrasia
0360-0172	EUPHRASIA OFFICINALIS	EUPHRASIA