Mid Valley Pharmaceutical

FDA Regulatory Profile

Mid Valley Pharmaceutical appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1136-2017, Class II) was initiated on August 30, 2017.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1136-2017Class IIDoctor Manzanilla Cough & Cold (diphenhydramine hydrochloride and phenylephrine hydrochloride) SyrupAugust 30, 2017
D-1135-2017Class IIDoctor Manzanilla Allergy & Decongestant Relief (diphenhydramine hydrochloride and phenylephrine hyAugust 30, 2017