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Ammonia Inhalants
Ammonia Inhalants - 39822-9900-2 - (Ammonia Inhalants)
Drug Information of Ammonia Inhalants
| Product NDC: | 39822-9900 |
| Proprietary Name: | Ammonia Inhalants |
| Non Proprietary Name: | Ammonia Inhalants |
| Active Ingredient(s): | .045 g/.3mL & nbsp; Ammonia Inhalants |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | INHALANT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ammonia Inhalants
| Product NDC: | 39822-9900 |
| Labeler Name: | X-GEN Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19760214 |
Package Information of Ammonia Inhalants
| Package NDC: | 39822-9900-2 |
| Package Description: | 12 AMPULE in 1 CARTON (39822-9900-2) > .3 mL in 1 AMPULE |
NDC Information of Ammonia Inhalants
| NDC Code | 39822-9900-2 |
| Proprietary Name | Ammonia Inhalants |
| Package Description | 12 AMPULE in 1 CARTON (39822-9900-2) > .3 mL in 1 AMPULE |
| Product NDC | 39822-9900 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ammonia Inhalants |
| Dosage Form Name | INHALANT |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 19760214 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | X-GEN Pharmaceuticals, Inc. |
| Substance Name | AMMONIA |
| Strength Number | .045 |
| Strength Unit | g/.3mL |
| Pharmaceutical Classes |
