NDC 49873-045

INON

Aluminum Hydroxide, Magnesium Carbonate, Sodium Bicarbonate

INON is a Oral Granule in the Human Otc Drug category. It is labeled and distributed by Sato Pharmaceutical Co., Ltd.. The primary component is Aluminum Hydroxide; Magnesium Carbonate; Sodium Bicarbonate.

• Product ID: 49873-045_55d0ad13-a37a-4366-b461-1d35195c1f93
• NDC: 49873-045
• Product Type: Human Otc Drug
• Proprietary Name: INON
• Generic Name: Aluminum Hydroxide, Magnesium Carbonate, Sodium Bicarbonate
• Dosage Form: Granule
• Route of Administration: ORAL
• Marketing Start Date: 1989-05-31
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part331
• Labeler Name: Sato Pharmaceutical Co., Ltd.
• Substance Name: ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE; SODIUM BICARBONATE
• Active Ingredient Strength: 400 mg/1.92g; mg/1.92g; mg/1.92g
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 49873-045-01

12 PACKET in 1 CARTON (49873-045-01) > 1.92 g in 1 PACKET

• Marketing Start Date: 1989-05-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 49873-045-01 [49873004501]

INON GRANULE

• Marketing Category: OTC monograph final
• Application Number: part331
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1989-05-31

Drug Details

Active Ingredients

Ingredient	Strength
ALUMINUM HYDROXIDE	400 mg/1.92g

OpenFDA Data

• SPL SET ID: e86d9c57-c877-49f1-a405-95a9a226ccf3
• Manufacturer:
  • Sato Pharmaceutical Co., Ltd.
• UNII:
  • 8MDF5V39QO
  • 0E53J927NA
  • 5QB0T2IUN0
• UPC Code:
  • 0349873045016