Product NDC: | 0074-1040 |
Proprietary Name: | Survanta |
Non Proprietary Name: | Beractant |
Active Ingredient(s): | 25 mg/mL & nbsp; Beractant |
Administration Route(s): | ENDOTRACHEAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0074-1040 |
Labeler Name: | AbbVie Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020032 |
Marketing Category: | NDA |
Start Marketing Date: | 19910701 |
Package NDC: | 0074-1040-04 |
Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (0074-1040-04) > 4 mL in 1 VIAL, SINGLE-USE |
NDC Code | 0074-1040-04 |
Proprietary Name | Survanta |
Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0074-1040-04) > 4 mL in 1 VIAL, SINGLE-USE |
Product NDC | 0074-1040 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Beractant |
Dosage Form Name | SUSPENSION |
Route Name | ENDOTRACHEAL |
Start Marketing Date | 19910701 |
Marketing Category Name | NDA |
Labeler Name | AbbVie Inc. |
Substance Name | BERACTANT |
Strength Number | 25 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Alveolar Surface Tension Reduction [PE],Surfactant [EPC],Surfactant Activity [MoA] |