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Ipratropium Bromide
Ipratropium Bromide - 0487-9801-01 - (Ipratropium Bromide)
Drug Information of Ipratropium Bromide
| Product NDC: | 0487-9801 |
| Proprietary Name: | Ipratropium Bromide |
| Non Proprietary Name: | Ipratropium Bromide |
| Active Ingredient(s): | .5 mg/2.5mL & nbsp; Ipratropium Bromide |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ipratropium Bromide
| Product NDC: | 0487-9801 |
| Labeler Name: | Nephron Pharmaceuticals Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075562 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010927 |
Package Information of Ipratropium Bromide
| Package NDC: | 0487-9801-01 |
| Package Description: | 30 POUCH in 1 CARTON (0487-9801-01) > 1 VIAL, SINGLE-DOSE in 1 POUCH > 2.5 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Ipratropium Bromide
| NDC Code | 0487-9801-01 |
| Proprietary Name | Ipratropium Bromide |
| Package Description | 30 POUCH in 1 CARTON (0487-9801-01) > 1 VIAL, SINGLE-DOSE in 1 POUCH > 2.5 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0487-9801 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ipratropium Bromide |
| Dosage Form Name | SOLUTION |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20010927 |
| Marketing Category Name | ANDA |
| Labeler Name | Nephron Pharmaceuticals Corporation |
| Substance Name | IPRATROPIUM BROMIDE |
| Strength Number | .5 |
| Strength Unit | mg/2.5mL |
| Pharmaceutical Classes |
