NDC 0360-0157

DROSERA

Drosera

DROSERA is a Sublingual Tablet in the Human Otc Drug category. It is labeled and distributed by Standard Homeopathic Company. The primary component is Drosera Anglica.

• Product ID: 0360-0157_7c4f2099-2fc8-5469-e053-2991aa0a48d3
• NDC: 0360-0157
• Product Type: Human Otc Drug
• Proprietary Name: DROSERA
• Generic Name: Drosera
• Dosage Form: Tablet
• Route of Administration: SUBLINGUAL
• Marketing Start Date: 1997-02-17
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: STANDARD HOMEOPATHIC COMPANY
• Substance Name: DROSERA ANGLICA
• Active Ingredient Strength: 6 [hp_X]/g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0360-0157-01

1 g in 1 BOTTLE, PLASTIC (0360-0157-01)

• Marketing Start Date: 1997-02-17
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0360-0157-01 [00360015701]

DROSERA TABLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1997-02-17

Drug Details

Active Ingredients

Ingredient	Strength
DROSERA ANGLICA	6 [hp_X]/g

OpenFDA Data

• SPL SET ID: 4c8683f3-6601-51db-e054-00144ff8d46c
• Manufacturer:
  • STANDARD HOMEOPATHIC COMPANY
• UNII:
  • J61BY05EGY
• UPC Code:
  • 0300360015714

NDC Crossover Matching brand name "DROSERA" or generic name "Drosera"

NDC	Brand Name	Generic Name
0220-1784	Drosera	DROSERA ROTUNDIFOLIA
0220-1785	Drosera	DROSERA ROTUNDIFOLIA
0220-1788	Drosera	DROSERA ROTUNDIFOLIA
0220-1792	Drosera	DROSERA ROTUNDIFOLIA
0220-1793	Drosera	DROSERA ROTUNDIFOLIA
0220-1796	Drosera	DROSERA ROTUNDIFOLIA
0220-1797	Drosera	DROSERA ROTUNDIFOLIA
0220-1800	Drosera	DROSERA ROTUNDIFOLIA
0220-1801	Drosera	DROSERA ROTUNDIFOLIA
0360-0156	DROSERA	DROSERA
0360-0157	DROSERA	DROSERA
53645-2000	Drosera	Drosera
62106-7919	DROSERA	Sundew
76472-4047	DROSERA	DROSERA
76472-4079	DROSERA	DROSERA