Pyrite

Product NDC
63083-8137
11-digit product format
630838137
Labeler code
63083
Product ID
63083-8137_41a2c1b2-c0d0-44f6-ba79-8e093311b86c
Type
HUMAN OTC DRUG
Nonproprietary name
Pyrite
Dosage form
LIQUID
Route
ORAL
Labeler
Professional Complementary Health Formulas
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1984-08-15
Marketing end
0000-00-00
Substance
FERROUS CATION
Active strength
6 [hp_X]/59mL
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-8137-22026-01-09C16284748780-11030e365-0b3c-111a-e063-dadaa90a10e2UPYR
63083-8137-22024-01-30C16284748780-11030e365-0b3c-111a-e063-dadaa90a10e2UPYR

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-8137PYRITE 8137 (PYRITE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Legacy NDC20220218_f0c8be60-8107-411f-8f41-196b1892db5c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-8137-26308381370259 mL in 1 BOTTLE, DROPPER (63083-8137-2) 59 ml1985-08-150000-00-00NoNoCurrent