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Nitrous Oxide - 21220-122-04 - (Nitrous Oxide)

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Drug Information of Nitrous Oxide

Product NDC: 21220-122
Proprietary Name: Nitrous Oxide
Non Proprietary Name: Nitrous Oxide
Active Ingredient(s): 995    mL/L & nbsp;   Nitrous Oxide
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): GAS
Coding System: National Drug Codes(NDC)

Labeler Information of Nitrous Oxide

Product NDC: 21220-122
Labeler Name: General Air Service & Supply Co
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED MEDICAL GAS
Start Marketing Date: 19761101

Package Information of Nitrous Oxide

Package NDC: 21220-122-04
Package Description: 7391 L in 1 CYLINDER (21220-122-04)

NDC Information of Nitrous Oxide

NDC Code 21220-122-04
Proprietary Name Nitrous Oxide
Package Description 7391 L in 1 CYLINDER (21220-122-04)
Product NDC 21220-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nitrous Oxide
Dosage Form Name GAS
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 19761101
Marketing Category Name UNAPPROVED MEDICAL GAS
Labeler Name General Air Service & Supply Co
Substance Name NITROUS OXIDE
Strength Number 995
Strength Unit mL/L
Pharmaceutical Classes

Complete Information of Nitrous Oxide


General Information