Plumeria Rubra

Product NDC
63545-686
11-digit product format
635450686
Labeler code
63545
Product ID
63545-686_4ebaa367-2c67-431b-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Plumeria Rubra
Dosage form
PELLET
Route
BUCCAL; ORAL; SUBLINGUAL
Labeler
Hahnemann Laboratories, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-05-04
Marketing end
0000-00-00
Substance
PLUMERIA RUBRA WHOLE
Active strength
30 [hp_C]/[hp_C]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63545-686-012020-01-31C16284748780-19d75b9d0-da56-f424-e053-dadaa90a57ce4ebaa367-2c66-431b-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63545-686-01Plumeria Rubra240 [hp_C] in 1 VIAL, GLASSPELLET2401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63545-686PLUMERIA RUBRA PELLET [HAHNEMANN LABORATORIES, INC.]1Legacy NDC, 1 package rows20170505_4ebaa367-2c66-431b-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
63545-686-0163545068601240 [hp_C] in 1 VIAL, GLASSHistorical