Details for New Drug Application (NDA): 208884
✉ Email this page to a colleague
NDA 208884 describes ALBUTEROL SULFATE, which is a drug marketed by Armstrong Pharms, Cipla, Lupin, Padagis Us, Sandoz, Actavis Mid Atlantic, Apotex Inc, Bausch, Copley Pharm, Epic Pharma Llc, Landela Pharm, Lexenpharm, Luoxin Aurovitas, Nephron, Norvium Bioscience, Ritedose Corp, Roxane, Sentiss, Sun Pharm, Teva Pharms, Watson Labs, Watson Labs Inc, Wockhardt Eu Operatn, Amneal Pharms, Chartwell Molecular, Chartwell Rx, Cosette, Hikma, Mova, Quagen, Teva, Rising, Aizant, Am Therap, Amneal Pharms Co, Aurobindo Pharma Ltd, Dash Pharms Natco, Hibrow Hlthcare, Pliva, Strides Pharma, Sun Pharm Industries, Ucb Inc, Virtus Pharm, Warner Chilcott, Zydus Pharms, Aiping Pharm Inc, and Watson Labs Teva, and is included in eighty-two NDAs. It is available from thirty-eight suppliers. Additional details are available on the ALBUTEROL SULFATE profile page.
The generic ingredient in ALBUTEROL SULFATE is albuterol sulfate; ipratropium bromide. There are thirty-eight drug master file entries for this compound. Fifteen suppliers are listed for this compound. Additional details are available on the albuterol sulfate; ipratropium bromide profile page.
The generic ingredient in ALBUTEROL SULFATE is albuterol sulfate; ipratropium bromide. There are thirty-eight drug master file entries for this compound. Fifteen suppliers are listed for this compound. Additional details are available on the albuterol sulfate; ipratropium bromide profile page.
Summary for 208884
| Tradename: | ALBUTEROL SULFATE |
| Applicant: | Zydus Pharms |
| Ingredient: | albuterol sulfate |
| Patents: | 0 |
Pharmacology for NDA: 208884
| Mechanism of Action | Adrenergic beta2-Agonists |
Suppliers and Packaging for NDA: 208884
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ALBUTEROL SULFATE | albuterol sulfate | TABLET;ORAL | 208884 | ANDA | Zydus Pharmaceuticals USA Inc. | 70710-1061 | 70710-1061-1 | 100 TABLET in 1 BOTTLE (70710-1061-1) |
| ALBUTEROL SULFATE | albuterol sulfate | TABLET;ORAL | 208884 | ANDA | Zydus Pharmaceuticals USA Inc. | 70710-1062 | 70710-1062-1 | 100 TABLET in 1 BOTTLE (70710-1062-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 2MG BASE | ||||
| Approval Date: | Oct 22, 2020 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 4MG BASE | ||||
| Approval Date: | Oct 22, 2020 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
