FATIGUE - 64117-199-02 - (LACTOSE, X-RAY EXPOSED (1000 RAD))

Alphabetical Index


Drug Information of FATIGUE

Product NDC: 64117-199
Proprietary Name: FATIGUE
Non Proprietary Name: LACTOSE, X-RAY EXPOSED (1000 RAD)
Active Ingredient(s): 30    [hp_C]/mL & nbsp;   LACTOSE, X-RAY EXPOSED (1000 RAD)
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of FATIGUE

Product NDC: 64117-199
Labeler Name: Natural Health Supply
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19980604

Package Information of FATIGUE

Package NDC: 64117-199-02
Package Description: 7.5 mL in 1 BOTTLE, GLASS (64117-199-02)

NDC Information of FATIGUE

NDC Code 64117-199-02
Proprietary Name FATIGUE
Package Description 7.5 mL in 1 BOTTLE, GLASS (64117-199-02)
Product NDC 64117-199
Product Type Name HUMAN OTC DRUG
Non Proprietary Name LACTOSE, X-RAY EXPOSED (1000 RAD)
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19980604
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natural Health Supply
Substance Name LACTOSE, X-RAY EXPOSED (1000 RAD)
Strength Number 30
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of FATIGUE


General Information