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Budesonide
Budesonide - 0093-6816-73 - (Budesonide)
Drug Information of Budesonide
| Product NDC: | 0093-6816 |
| Proprietary Name: | Budesonide |
| Non Proprietary Name: | Budesonide |
| Active Ingredient(s): | .5 mg/2mL & nbsp; Budesonide |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Budesonide
| Product NDC: | 0093-6816 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077519 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081119 |
Package Information of Budesonide
| Package NDC: | 0093-6816-73 |
| Package Description: | 6 POUCH in 1 CARTON (0093-6816-73) > 5 VIAL, SINGLE-DOSE in 1 POUCH (0093-6816-45) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Budesonide
| NDC Code | 0093-6816-73 |
| Proprietary Name | Budesonide |
| Package Description | 6 POUCH in 1 CARTON (0093-6816-73) > 5 VIAL, SINGLE-DOSE in 1 POUCH (0093-6816-45) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0093-6816 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Budesonide |
| Dosage Form Name | SUSPENSION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20081119 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | BUDESONIDE |
| Strength Number | .5 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
