NDC 48883-006

Helium

Helium

Helium is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Encompass Medical & Specialty Gases, Ltd.. The primary component is Helium.

• Product ID: 48883-006_6c805a0d-190e-4913-8773-189291f0161d
• NDC: 48883-006
• Product Type: Human Prescription Drug
• Proprietary Name: Helium
• Generic Name: Helium
• Dosage Form: Gas
• Route of Administration: RESPIRATORY (INHALATION)
• Marketing Start Date: 2009-04-15
• Marketing Category: UNAPPROVED MEDICAL GAS / UNAPPROVED MEDICAL GAS
• Labeler Name: Encompass Medical & Specialty Gases, Ltd.
• Substance Name: HELIUM
• Active Ingredient Strength: 990 mL/L
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 48883-006-03

377 L in 1 CYLINDER (48883-006-03)

• Marketing Start Date: 2009-04-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 48883-006-04 [48883000604]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-15
• Inactivation Date: 2019-10-29

NDC 48883-006-05 [48883000605]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-15
• Inactivation Date: 2019-10-29

NDC 48883-006-02 [48883000602]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-15
• Inactivation Date: 2019-10-29

NDC 48883-006-03 [48883000603]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-15
• Inactivation Date: 2019-10-29

NDC 48883-006-01 [48883000601]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-15
• Inactivation Date: 2019-10-29

NDC 48883-006-06 [48883000606]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-15
• Inactivation Date: 2019-10-29

NDC 48883-006-07 [48883000607]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-04-15
• Inactivation Date: 2019-10-29

Drug Details

Active Ingredients

Ingredient	Strength
HELIUM	990 mL/L

OpenFDA Data

• SPL SET ID: a7a73da7-a15b-4216-b4a7-c24fcafd201f
• Manufacturer:
  • Encompass Medical & Specialty Gases, Ltd.
• UNII:
  • 206GF3GB41
• RxNorm Concept Unique ID - RxCUI:
  • 310693

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

NDC	Brand Name	Generic Name
10006-008	HELIUM	HELIUM
10014-004	Helium	Helium
10018-9505	Helium	Helium
10167-300	HELIUM	HELIUM
10297-006	Helium	Helium
10678-004	Helium	Helium
10736-020	Helium	Helium
11054-004	HELIUM	HELIUM
11324-005	Helium	Helium
12213-710	Helium	Helium
14961-005	Helium	Helium
17575-005	Helium	Helium
21220-121	Helium	Helium
25543-011	Helium	Helium
25373-010	Helium	Helium
42602-002	HELIUM	HELIUM
46123-008	Helium	Helium
48883-006	Helium	Helium
54416-005	Helium	Helium
55037-501	Helium	Helium
57472-007	Helium	Helium
58420-004	Helium	Helium
58789-005	Helium	Helium
59579-005	Helium	Helium
61095-300	Helium	Helium
48273-011	Helium	Helium
73468-002	Helium	Helium
51486-020	Helium	Helium