Amber

Product NDC
63083-8103
11-digit product format
630838103
Labeler code
63083
Product ID
63083-8103_92e9ff34-2cb6-4985-82c2-aa88340e5bba
Type
HUMAN OTC DRUG
Nonproprietary name
Amber
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
AMBER
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
63083-8103-22026-01-08C16284748780-11030e365-0f5e-111a-e063-dadaa90a10e2UAMB
63083-8103-22024-01-30C16284748780-11030e365-0f5e-111a-e063-dadaa90a10e2UAMB

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-8103AMBER 8103 (AMBER) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Legacy NDC20220216_e622700e-d87e-43d4-9327-4d2260a3c71c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63083-8103-26308381030259 mL in 1 BOTTLE, DROPPER (63083-8103-2) 59 ml1985-08-150000-00-00NoNoCurrent