NDC 48951-9999

Sucrose

Sucrose

Sucrose is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc. The primary component is Sucrose.

• Product ID: 48951-9999_b5cb3250-1038-11df-8a39-0800200c9a66
• NDC: 48951-9999
• Product Type: Human Otc Drug
• Proprietary Name: Sucrose
• Generic Name: Sucrose
• Dosage Form: Pellet
• Route of Administration: ORAL
• Marketing Start Date: 2010-02-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Uriel Pharmacy Inc
• Substance Name: SUCROSE
• Active Ingredient Strength: 1 [hp_X]/1
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 48951-9999-2

1350 PELLET in 1 BOTTLE, GLASS (48951-9999-2)

• Marketing Start Date: 2010-02-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48951-9999-2 [48951999902]

Sucrose PELLET

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-02-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SUCROSE	1 [hp_X]/1

OpenFDA Data

• SPL SET ID: fa4e4ce0-1039-11df-8a39-0800200c9a66
• Manufacturer:
  • Uriel Pharmacy Inc
• UNII:
  • C151H8M554

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

NDC	Brand Name	Generic Name
48951-9999	Sucrose	SUCROSE
58264-0297	A-5	SUCROSE
64117-282	DYSPEPSIA HEADACHE	SUCROSE
0220-4522	Saccharum officinale	SUCROSE
0220-4531	Saccharum officinale	SUCROSE
0220-4532	Saccharum officinale	SUCROSE
68428-614	Saccharum officinale	SUCROSE
71919-601	Saccharum officinale	SUCROSE