NDC 51662-1331

RINGERS

Sodium Lactate, Potassium Chloride, Sodium Chloride, Calcium Chloride

RINGERS is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Sodium Lactate; Potassium Chloride; Calcium Chloride; Sodium Chloride.

• Product ID: 51662-1331_78bf664e-df34-cda9-e053-2a91aa0a5a06
• NDC: 51662-1331
• Product Type: Human Prescription Drug
• Proprietary Name: RINGERS
• Generic Name: Sodium Lactate, Potassium Chloride, Sodium Chloride, Calcium Chloride
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2018-10-21
• Marketing Category: NDA / NDA
• Application Number: NDA017641
• Labeler Name: HF Acquisition Co LLC, DBA HealthFirst
• Substance Name: SODIUM LACTATE; POTASSIUM CHLORIDE; CALCIUM CHLORIDE; SODIUM CHLORIDE
• Active Ingredient Strength: 310 mg/100mL; mg/100mL; mg/100mL; mg/100mL
• Pharm Classes: Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 51662-1331-1

1 BAG in 1 POUCH (51662-1331-1) > 1000 mL in 1 BAG

• Marketing Start Date: 2018-10-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51662-1331-1 [51662133101]

RINGERS INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA017641
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-10-21
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-02-07

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM LACTATE	310 mg/100mL

OpenFDA Data

• SPL SET ID: 78bf664e-df33-cda9-e053-2a91aa0a5a06
• Manufacturer:
  • HF Acquisition Co LLC, DBA HealthFirst
• UNII:
  • TU7HW0W0QT
  • M4I0D6VV5M
  • 451W47IQ8X
  • 660YQ98I10
• RxNorm Concept Unique ID - RxCUI:
  • 847630

Pharmacological Class

• Osmotic Laxative [EPC]
• Increased Large Intestinal Motility [PE]
• Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
• Osmotic Activity [MoA]
• Potassium Compounds [CS]
• Potassium Salt [EPC]
• Osmotic Laxative [EPC]
• Increased Large Intestinal Motility [PE]
• Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
• Osmotic Activity [MoA]
• Blood Coagulation Factor [EPC]
• Increased Coagulation Factor Activity [PE]
• Calcium [CS]
• Cations
• Divalent [CS]
• Osmotic Laxative [EPC]
• Increased Large Intestinal Motility [PE]
• Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
• Osmotic Activity [MoA]

NDC Crossover Matching brand name "RINGERS" or generic name "Sodium Lactate, Potassium Chloride, Sodium Chloride, Calcium Chloride"

NDC	Brand Name	Generic Name
0264-2202	Ringers	Sodium Chloride, Potassium Chloride, and Calcium Chloride
0264-7780	Ringers	Sodium Chloride, Calcium Chloride, and Potassium Chloride
0338-0104	Ringers	sodium chloride, calcium chloride, potassium chloride,
0338-0105	Ringers	Sodium Chloride, Calcium Chloride, Potassium Chloride
0409-6140	Ringers	SODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE
0409-7982	Ringers	SODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE
0990-7982	Ringers	SODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE
51662-1331	RINGERS	SODIUM LACTATE, POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE