NDC 50063-003

Air

Air

Air is a Respiratory (inhalation) Gas in the Human Prescription Drug category. It is labeled and distributed by Andy-oxy Co., Inc.. The primary component is Air.

• Product ID: 50063-003_40e3a56e-cc6b-4f13-b36c-a905108423fa
• NDC: 50063-003
• Product Type: Human Prescription Drug
• Proprietary Name: Air
• Generic Name: Air
• Dosage Form: Gas
• Route of Administration: RESPIRATORY (INHALATION)
• Marketing Start Date: 2007-01-01
• Marketing Category: UNAPPROVED MEDICAL GAS / UNAPPROVED MEDICAL GAS
• Labeler Name: Andy-Oxy Co., Inc.
• Substance Name: AIR
• Active Ingredient Strength: 1000 mL/L
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 50063-003-07

9345 L in 1 CYLINDER (50063-003-07)

• Marketing Start Date: 2007-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50063-003-03 [50063000303]

Air GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-01-01
• Inactivation Date: 2019-11-27

NDC 50063-003-05 [50063000305]

Air GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-01-01
• Inactivation Date: 2019-11-27

NDC 50063-003-01 [50063000301]

Air GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-01-01
• Inactivation Date: 2019-11-27

NDC 50063-003-04 [50063000304]

Air GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-01-01
• Inactivation Date: 2019-11-27

NDC 50063-003-02 [50063000302]

Air GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-01-01
• Inactivation Date: 2019-11-27

NDC 50063-003-06 [50063000306]

Air GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-01-01
• Inactivation Date: 2019-11-27

NDC 50063-003-07 [50063000307]

Air GAS

• Marketing Category: unapproved medical gas
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2007-01-01
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
AIR	1000 mL/L

OpenFDA Data

• SPL SET ID: 0cd7fe2f-bbed-4726-bc93-5efee5e5425a
• Manufacturer:
  • Andy-Oxy Co., Inc.
• UNII:
  • K21NZZ5Y0B

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

NDC	Brand Name	Generic Name
10218-003	Air	Breathing Air
10297-003	Air	Air
10297-005	Air	Air
10297-103	Air	Air
10451-002	Air	Air
10451-004	Air	Air
10678-005	Air	Air
10736-016	AIR	AIR
10927-104	AIR	AIR
11054-110	Air	Air
11324-006	Air	Air
11564-003	Air	Air
11564-004	Air	Air
12213-700	Air	Air
70151-003	Air	Air
14961-004	Air	Air
17575-007	Air	Air
18482-004	Air	Air
21220-152	Air	Air
17575-300	Air	Air
21220-124	Air	Air
23647-003	Air	Air
25543-005	Air	Air
34057-006	Air	Air
42241-003	Air	Air
43621-004	Air	Air
46123-009	Air	Air
48883-005	Air	Air
49204-003	AIR	AIR
49204-004	Air	Air
49575-004	Air	Air
50063-004	Air	Air
50063-003	Air	Air
49972-006	Air	Air
50554-007	Air	Air
51012-003	AIR	AIR
51486-018	Air	Air
51486-004	Air	Air
51887-502	Air	Air
52346-014	Air	Air
53440-007	Air	Air
53440-005	Air	Air
53452-003	Air	Air
55037-302	Air	Air
54416-004	Air	Air
55147-004	Air	Air
55749-007	Air	Air
57472-006	AIR	AIR
58356-003	Air	Air
58420-005	Air	Air