← FDA Drug Approvals (Drugs@FDA)
MAPROTILINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: HERITAGE PHARMA · Approved 1988-06-01
Drug application
- FDA Application #
ANDA072162- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- MAPROTILINE HYDROCHLORIDE
- Generic name
- Maprotiline Hydrochloride
- Active ingredients
- MAPROTILINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- HERITAGE PHARMA
- First approval
- 1988-06-01
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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