← FDA Drug Approvals (Drugs@FDA)
NEBIVOLOL HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: MANKIND PHARMA · Approved 2022-11-14
Drug application
- FDA Application #
ANDA216172- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- NEBIVOLOL HYDROCHLORIDE
- Generic name
- NEBIVOLOL
- Active ingredients
- NEBIVOLOL HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- MANKIND PHARMA
- Manufacturer
- Lifestar Pharma LLC
- First approval
- 2022-11-14
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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