NDC 54162-700

Sorbitol

Sorbitol

Sorbitol is a Oral Solution in the Human Otc Drug category. It is labeled and distributed by Geritrex Llc. The primary component is Sorbitol.

• Product ID: 54162-700_f0aa7245-b91f-499c-b009-77b00e41c9c8
• NDC: 54162-700
• Product Type: Human Otc Drug
• Proprietary Name: Sorbitol
• Generic Name: Sorbitol
• Dosage Form: Solution
• Route of Administration: ORAL
• Marketing Start Date: 2012-07-17
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part334
• Labeler Name: Geritrex LLC
• Substance Name: SORBITOL
• Active Ingredient Strength: 258 g/474mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 54162-700-16

474 mL in 1 BOTTLE, PLASTIC (54162-700-16)

• Marketing Start Date: 2015-07-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 54162-700-30 [54162070030]

Sorbitol SOLUTION

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Billing Unit: ML
• Marketing Start Date: 2015-07-31
• Inactivation Date: 2020-01-31

NDC 54162-700-16 [54162070016]

Sorbitol SOLUTION

• Marketing Category: OTC monograph not final
• Application Number: part334
• Product Type: HUMAN OTC DRUG
• Billing Unit: ML
• Marketing Start Date: 2015-07-31
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SORBITOL	258.2 g/474mL

OpenFDA Data

• SPL SET ID: ae9a1c12-8662-4f5d-8435-e51dc2b45780
• Manufacturer:
  • Geritrex LLC
• UNII:
  • 506T60A25R
• RxNorm Concept Unique ID - RxCUI:
  • 313092
• UPC Code:
  • 0354162700163
  • 0354162700309

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

NDC	Brand Name	Generic Name
0264-2301	Sorbitol	Sorbitol
0338-0295	Sorbitol	Sorbitol
52471-111	Sorbitol	Sorbitol
54162-700	Sorbitol	Sorbitol
57896-435	SORBITOL	sorbitol
57896-758	GeriCare Sorbitol Solution	Sorbitol