RUMEX CRISPUS

Product NDC
15631-0672
11-digit product format
156310672
Labeler code
15631
Product ID
15631-0672_ec0bc9f2-abfb-4753-92e5-9e1fb894aef6
Type
HUMAN OTC DRUG
Nonproprietary name
RUMEX CRISPUS
Dosage form
TABLET
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-12-27
Marketing end
0000-00-00
Substance
RUMEX CRISPUS ROOT
Active strength
1 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-0672-0RUMEX CRISPUS1 in 1 BLISTER PACKTABLET11
15631-0672-1RUMEX CRISPUS4 in 1 BLISTER PACKTABLET41
15631-0672-2RUMEX CRISPUS50 in 1 CONTAINERTABLET501
15631-0672-3RUMEX CRISPUS100 in 1 CONTAINERTABLET1001
15631-0672-4RUMEX CRISPUS250 in 1 CONTAINERTABLET2501
15631-0672-5RUMEX CRISPUS500 in 1 CONTAINERTABLET5001
15631-0672-6RUMEX CRISPUS1000 in 1 CONTAINERTABLET10001
15631-0672-7RUMEX CRISPUS10000 in 1 CONTAINERTABLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-0672RUMEX CRISPUS TABLET [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Legacy NDC, 8 package rows20151229_96d54449-3254-4844-8405-04b3282c690f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
15631-0672-0156310672001 in 1 BLISTER PACKHistorical
15631-0672-1156310672014 in 1 BLISTER PACKHistorical
15631-0672-21563106720250 in 1 CONTAINERHistorical
15631-0672-315631067203100 in 1 CONTAINERHistorical
15631-0672-415631067204250 in 1 CONTAINERHistorical
15631-0672-515631067205500 in 1 CONTAINERHistorical
15631-0672-6156310672061000 in 1 CONTAINERHistorical
15631-0672-71563106720710000 in 1 CONTAINERHistorical