NDC 66096-749

Spongilla lacustris MT

Spongilla Lacustris

Spongilla lacustris MT is a Oral Tincture in the Human Prescription Drug category. It is labeled and distributed by Ohm Pharma Inc.. The primary component is Spongilla Lacustris.

• Product ID: 66096-749_b8a7b0c8-25d0-5d2c-e053-2995a90a0006
• NDC: 66096-749
• Product Type: Human Prescription Drug
• Proprietary Name: Spongilla lacustris MT
• Generic Name: Spongilla Lacustris
• Dosage Form: Tincture
• Route of Administration: ORAL
• Marketing Start Date: 2019-03-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: OHM PHARMA INC.
• Substance Name: SPONGILLA LACUSTRIS
• Active Ingredient Strength: 1 [hp_X]/.25L
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 66096-749-08

.25 L in 1 BOTTLE (66096-749-08)

• Marketing Start Date: 2019-03-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 66096-749-08 [66096074908]

Spongilla lacustris MT TINCTURE

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-03-01

Drug Details

Active Ingredients

Ingredient	Strength
SPONGILLA LACUSTRIS	1 [hp_X]/.25L

OpenFDA Data

• SPL SET ID: a855d4ca-52ed-4e69-93b5-7304bcc84f73
• Manufacturer:
  • OHM PHARMA INC.
• UNII:
  • 6SZ0G98BHM

NDC Crossover Matching brand name "Spongilla lacustris MT" or generic name "Spongilla Lacustris"

NDC	Brand Name	Generic Name
66096-749	Spongilla lacustris MT	Spongilla lacustris
0220-0759	Badiaga	SPONGILLA LACUSTRIS
0220-0761	Badiaga	SPONGILLA LACUSTRIS
68428-246	Badiaga	SPONGILLA LACUSTRIS
71919-107	Badiaga	SPONGILLA LACUSTRIS