NDC 51662-1520

0.9% SODIUM CHLORIDE

0.9% Sodium Chloride

0.9% SODIUM CHLORIDE 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 Chloride.

• Product ID: 51662-1520_a62b71db-8ba3-6f6b-e053-2a95a90a29d1
• NDC: 51662-1520
• Product Type: Human Prescription Drug
• Proprietary Name: 0.9% SODIUM CHLORIDE
• Generic Name: 0.9% Sodium Chloride
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2020-05-21
• Marketing Category: NDA / NDA
• Application Number: NDA016366
• Labeler Name: HF Acquisition Co LLC, DBA HealthFirst
• Substance Name: SODIUM CHLORIDE
• Active Ingredient Strength: 900 mg/100mL
• Pharm Classes: 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: 2021-12-31

Packaging

NDC 51662-1520-1

100 mL in 1 BAG (51662-1520-1)

• Marketing Start Date: 2020-05-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51662-1520-1 [51662152001]

0.9% SODIUM CHLORIDE INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA016366
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2020-05-21

Drug Details

NDC Crossover Matching brand name "0.9% SODIUM CHLORIDE" or generic name "0.9% Sodium Chloride"

NDC	Brand Name	Generic Name
51662-1260	0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE
51662-1301	0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE
51662-1308	0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE
51662-1359	0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE
51662-1517	0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE
51662-1518	0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE
51662-1520	0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE
51662-1577	0.9% SODIUM CHLORIDE	SODIUM CHLORIDE
51662-1609	0.9% SODIUM CHLORIDE	0.9% SODIUM CHLORIDE