NDC 10019-651

Sevoflurane

Sevoflurane

Sevoflurane is a Respiratory (inhalation) Liquid in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Sevoflurane.

• Product ID: 10019-651_075499ae-75f0-4f96-8eb5-40bd8bf0d8fb
• NDC: 10019-651
• Product Type: Human Prescription Drug
• Proprietary Name: Sevoflurane
• Generic Name: Sevoflurane
• Dosage Form: Liquid
• Route of Administration: RESPIRATORY (INHALATION)
• Marketing Start Date: 2002-07-02
• Marketing Category: ANDA / ANDA
• Application Number: ANDA075895
• Labeler Name: Baxter Healthcare Corporation
• Substance Name: SEVOFLURANE
• Active Ingredient Strength: 250 mL/250mL
• Pharm Classes: General Anesthesia [PE], General Anesthetic [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 10019-651-64

6 BOTTLE in 1 CARTON (10019-651-64) > 250 mL in 1 BOTTLE

• Marketing Start Date: 2002-07-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10019-651-64 [10019065164]

Sevoflurane LIQUID

• Marketing Category: ANDA
• Application Number: ANDA075895
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2002-07-02

Drug Details

Active Ingredients

Ingredient	Strength
SEVOFLURANE	250 mL/250mL

OpenFDA Data

• SPL SET ID: ea8bf997-2c71-4014-b18d-4f7ab45dfa19
• Manufacturer:
  • Baxter Healthcare Corporation
• UNII:
  • 38LVP0K73A
• RxNorm Concept Unique ID - RxCUI:
  • 200243

Pharmacological Class

• General Anesthesia [PE]
• General Anesthetic [EPC]

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

NDC	Brand Name	Generic Name
0781-6160	Sevoflurane	Sevoflurane
10019-651	Sevoflurane	Sevoflurane
10019-653	SEVOFLURANE	Sevoflurane
10019-655	Sevoflurane	Sevoflurane
10019-657	SEVOFLURANE	Sevoflurane
12164-005	Sevoflurane	sevoflurane
66794-015	Sevoflurane	Sevoflurane
66794-022	Sevoflurane	Sevoflurane
66794-012	Sojourn	Sevoflurane
0074-4456	Ultane	Sevoflurane