NDC 58420-004

Helium

Helium

Helium is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Airgas Intermountain Inc. The primary component is Helium.

• Product ID: 58420-004_17eaf086-da43-45a9-96f7-4963599d8041
• NDC: 58420-004
• Product Type: Human Prescription Drug
• Proprietary Name: Helium
• Generic Name: Helium
• Dosage Form: Gas
• Route of Administration: RESPIRATORY (INHALATION)
• Marketing Start Date: 1985-01-01
• Marketing Category: UNAPPROVED MEDICAL GAS / UNAPPROVED MEDICAL GAS
• Labeler Name: Airgas Intermountain Inc
• Substance Name: HELIUM
• Active Ingredient Strength: 992 mL/L
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 58420-004-10

5493 L in 1 CYLINDER (58420-004-10)

• Marketing Start Date: 1985-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58420-004-03 [58420000403]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-10 [58420000410]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-09 [58420000409]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-06 [58420000406]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-08 [58420000408]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-01 [58420000401]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-04 [58420000404]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-02 [58420000402]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-07 [58420000407]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-05 [58420000405]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

NDC 58420-004-11 [58420000411]

Helium GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1985-01-01
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
HELIUM	992 mL/L

OpenFDA Data

• SPL SET ID: 11fda4bb-5a9f-4633-925c-db7bbbf9c2cf
• Manufacturer:
  • Airgas Intermountain Inc
• UNII:
  • 206GF3GB41
• RxNorm Concept Unique ID - RxCUI:
  • 997972

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