Labetalol hydrochloride - Labetalol hydrochloride
Navigation: NDC > Supplier starting with: W > WATSON LABORATORIES, INC.| Field | Value |
|---|---|
| NDC Code: | 0591-0605 |
| Proprietary Name: | Labetalol hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Labetalol hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 03-08-1998 |
| Category Name: | ANDA |
| Application Number: | ANDA075133 |
| Labeler: | WATSON LABORATORIES, INC. |
| Substance Name: | LABETALOL HYDROCHLORIDE |
| Active Numerator Strength: | 100 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
| DEA Schedule: |