← FDA Drug Approvals (Drugs@FDA)
NAFTIFINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA CANADA · Approved 2019-04-10
Drug application
- FDA Application #
ANDA208201- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- NAFTIFINE HYDROCHLORIDE
- Generic name
- NAFTIFINE HYDROCHLORIDE
- Active ingredients
- NAFTIFINE HYDROCHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Marketing status
- Prescription
- Sponsor
- SUN PHARMA CANADA
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- First approval
- 2019-04-10
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown