KALI SULPH

Product NDC
54973-3107
11-digit product format
549733107
Labeler code
54973
Product ID
54973-3107_60403e9f-7e10-05cb-e053-2991aa0a64f2
Type
HUMAN OTC DRUG
Nonproprietary name
potassium sulfate
Dosage form
TABLET
Route
ORAL
Labeler
Hyland's
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1940-01-01
Marketing end
0000-00-00
Substance
POTASSIUM SULFATE
Active strength
30 [hp_X]/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
54973-3107-154973310701500 TABLET in 1 BOTTLE, PLASTIC (54973-3107-1) 500 tablet1940-01-010000-00-00NoNoCurrent