NDC 48951-6012

Lachesis Belladonna

Lachesis Belladonna

Lachesis Belladonna is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Atropa Belladonna; Mercurialis Perennis; Calcium Sulfide; Lachesis Muta Venom.

• Product ID: 48951-6012_6d6cc2d3-e522-a7a7-e053-2a91aa0aad96
• NDC: 48951-6012
• Product Type: Human Otc Drug
• Proprietary Name: Lachesis Belladonna
• Generic Name: Lachesis Belladonna
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2009-09-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Uriel Pharmacy Inc.
• Substance Name: ATROPA BELLADONNA; MERCURIALIS PERENNIS; CALCIUM SULFIDE; LACHESIS MUTA VENOM
• Active Ingredient Strength: 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-6012-1

10 AMPULE in 1 BOX (48951-6012-1) > 1 mL in 1 AMPULE

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

NDC SPL Data Element Entries

NDC 48951-6012-1 [48951601201]

Lachesis Belladonna LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
ATROPA BELLADONNA	4 [hp_X]/mL

OpenFDA Data

• SPL SET ID: c617a849-5043-43cd-974f-2f0d664fd468
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • WQZ3G9PF0H
  • Q35465A1MA
  • 1MBW07J51Q
  • VSW71SS07I

NDC Crossover Matching brand name "Lachesis Belladonna" or generic name "Lachesis Belladonna"

NDC	Brand Name	Generic Name
48951-6012	Lachesis Belladonna	Lachesis Belladonna
48951-6013	Lachesis Belladonna	Lachesis Belladonna
48951-6014	Lachesis Belladonna	Lachesis Belladonna