NDC 46123-008

Helium

Helium

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

• Product ID: 46123-008_982ea3b6-ac8d-b5e8-e053-2a95a90ae558
• NDC: 46123-008
• Product Type: Human Prescription Drug
• Proprietary Name: Helium
• Generic Name: Helium
• Dosage Form: Gas
• Route of Administration: RESPIRATORY (INHALATION)
• Marketing Start Date: 1967-01-01
• Marketing Category: NDA / NDA
• Application Number: NDA205864
• Labeler Name: Roberts Oxygen Company, Inc.
• Substance Name: HELIUM
• Active Ingredient Strength: 990 mL/L
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 46123-008-01

102 L in 1 CYLINDER (46123-008-01)

• Marketing Start Date: 1967-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 46123-008-01 [46123000801]

Helium GAS

• Marketing Category: NDA
• Application Number: NDA205864
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1967-01-01

NDC 46123-008-03 [46123000803]

Helium GAS

• Marketing Category: NDA
• Application Number: NDA205864
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1967-01-01

NDC 46123-008-05 [46123000805]

Helium GAS

• Marketing Category: NDA
• Application Number: NDA205864
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1967-01-01

NDC 46123-008-04 [46123000804]

Helium GAS

• Marketing Category: NDA
• Application Number: NDA205864
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1967-01-01

NDC 46123-008-07 [46123000807]

Helium GAS

• Marketing Category: NDA
• Application Number: NDA205864
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1967-01-01

NDC 46123-008-02 [46123000802]

Helium GAS

• Marketing Category: NDA
• Application Number: NDA205864
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1967-01-01

NDC 46123-008-06 [46123000806]

Helium GAS

• Marketing Category: NDA
• Application Number: NDA205864
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 1967-01-01

Drug Details

Active Ingredients

Ingredient	Strength
HELIUM	990 mL/L

OpenFDA Data

• SPL SET ID: 554faa48-7fc2-4d1a-b223-82cf107b144f
• Manufacturer:
  • Roberts Oxygen Company, Inc.
• 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