Levalbuterol is a Respiratory (inhalation) Solution in the Human Prescription Drug category. It is labeled and distributed by Ritedose Pharmaceuticals,. The primary component is Levalbuterol Hy.
| Product ID | 76204-700_7d4dd0e8-6b46-38a3-e053-2991aa0a7fee | 
| NDC | 76204-700 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | Levalbuterol | 
| Generic Name | Levalbuterol Hydrochloride | 
| Dosage Form | Solution | 
| Route of Administration | RESPIRATORY (INHALATION) | 
| Marketing Start Date | 2016-03-22 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA203653 | 
| Labeler Name | Ritedose Pharmaceuticals, | 
| Substance Name | LEVALBUTEROL HY | 
| Active Ingredient Strength | 0 mg/3mL | 
| Pharm Classes | Adrenergic beta | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2019-12-31 | 
| Marketing Start Date | 2017-02-17 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA203653 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2017-02-17 | 
| Marketing Category | ANDA | 
| Application Number | ANDA203653 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2017-03-03 | 
| Marketing Category | ANDA | 
| Application Number | ANDA203653 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | ML | 
| Marketing Start Date | 2017-02-17 | 
| Marketing Category | ANDA | 
| Application Number | ANDA203653 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | ML | 
| Marketing Start Date | 2017-02-17 | 
| Marketing End Date | 2019-04-09 | 
| Marketing Category | ANDA | 
| Application Number | ANDA203653 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | ML | 
| Marketing Start Date | 2017-03-03 | 
| Marketing Category | ANDA | 
| Application Number | ANDA203653 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | ML | 
| Marketing Start Date | 2016-03-22 | 
| Marketing End Date | 2019-04-09 | 
| Marketing Category | ANDA | 
| Application Number | ANDA203653 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | ML | 
| Marketing Start Date | 2017-02-17 | 
| Marketing Category | ANDA | 
| Application Number | ANDA203653 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | ML | 
| Marketing Start Date | 2017-03-03 | 
| Ingredient | Strength | 
|---|---|
| LEVALBUTEROL HYDROCHLORIDE | .31 mg/3mL | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 0093-4145 | Levalbuterol | Levalbuterol | 
| 0093-4146 | Levalbuterol | Levalbuterol | 
| 0093-4147 | Levalbuterol | Levalbuterol | 
| 0093-4148 | Levalbuterol | Levalbuterol | 
| 0115-9930 | Levalbuterol | Levalbuterol Hydrochloride | 
| 0115-9931 | Levalbuterol | Levalbuterol Hydrochloride | 
| 0115-9932 | Levalbuterol | Levalbuterol Hydrochloride | 
| 0378-6993 | Levalbuterol | levalbuterol | 
| 0378-9680 | Levalbuterol | levalbuterol | 
| 0378-9681 | Levalbuterol | levalbuterol | 
| 0378-9682 | Levalbuterol | levalbuterol | 
| 0378-9690 | Levalbuterol | Levalbuterol | 
| 0378-9691 | Levalbuterol | Levalbuterol | 
| 0378-9692 | Levalbuterol | Levalbuterol | 
| 68788-6777 | Levalbuterol | Levalbuterol | 
| 76204-900 | Levalbuterol | Levalbuterol | 
| 76204-800 | Levalbuterol | Levalbuterol | 
| 76204-700 | Levalbuterol | Levalbuterol | 
| 63187-953 | Levalbuterol | Levalbuterol | 
| 65862-944 | Levalbuterol | Levalbuterol | 
| 65862-942 | LEVALBUTEROL | LEVALBUTEROL | 
| 65862-945 | Levalbuterol | Levalbuterol | 
| 65862-943 | Levalbuterol | Levalbuterol | 
| 68071-5027 | Levalbuterol | Levalbuterol | 
| 68071-2340 | Levalbuterol | Levalbuterol | 
| 17478-171 | Xopenex | Levalbuterol Hydrochloride | 
| 17478-172 | Xopenex | Levalbuterol Hydrochloride | 
| 17478-173 | Xopenex | Levalbuterol Hydrochloride | 
| 17478-174 | Xopenex | Levalbuterol Hydrochloride | 
| 21695-153 | Xopenex | levalbuterol hydrochloride |