NDC 48951-8208

Stannum Succinum

Stannum Succinum

Stannum Succinum is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Amber; Tin.

• Product ID: 48951-8208_6c421a6d-faae-139b-e053-2a91aa0a1ac2
• NDC: 48951-8208
• Product Type: Human Otc Drug
• Proprietary Name: Stannum Succinum
• Generic Name: Stannum Succinum
• 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: AMBER; TIN
• Active Ingredient Strength: 6 [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 48951-8208-1

1 BOTTLE, DROPPER in 1 BAG (48951-8208-1) > 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 48951-8208-1 [48951820801]

Stannum Succinum LIQUID

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

Drug Details

Active Ingredients

Ingredient	Strength
AMBER	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: c8b6c6eb-abc1-4390-85f4-e7a7d08f63e4
• Manufacturer:
  • Uriel Pharmacy Inc.
• UNII:
  • 387GMG9FH5
  • 70J9Z0J26P

NDC Crossover Matching brand name "Stannum Succinum" or generic name "Stannum Succinum"

NDC	Brand Name	Generic Name
48951-8208	Stannum Succinum	Stannum Succinum
48951-8365	Stannum Succinum	Stannum Succinum