General MedicationsORALGeneric
GRIFULVIN V
GRISEOFULVIN, MICROCRYSTALLINE
Standard Dose
125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Key Takeaways
- Primary indication: Marketing status: Discontinued
- Approval overview GRIFULVIN V is listed in Drugs@FDA under application 050448 (NDA).
- Marketing status: Discontinued Active ingredient GRISEOFULVIN, MICROCRYSTALLINE Form and strength SUSPENSION;ORAL - 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor JOHNSON AND JOHNSON Submission history Latest submission status date: 1998-10-08 00:00:00.
Structured Monograph
Clinical summary
Approval overview GRIFULVIN V is listed in Drugs@FDA under application 050448 (NDA). Marketing status: Discontinued Active ingredient GRISEOFULVIN, MICROCRYSTALLINE Form and strength SUSPENSION;ORAL - 125MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor JOHNSON AND JOHNSON Submission history Latest submission status date: 1998-10-08 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.