Medorrhinum

Product NDC
0220-7310
11-digit product format
002207310
Labeler code
0220
Product ID
0220-7310_0a35df43-5bfe-c58f-e063-6294a90aa4e0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
GONORRHEAL URETHRAL SECRETION HUMAN
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
GONORRHEAL URETHRAL SECRETION HUMAN
Active strength
15 [hp_C]/15[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Medorrhinum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GONORRHEAL URETHRAL SECRETION HUMAN15 [hp_C]/15[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9BZG9E3I8F

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-7310-412023-11-15C16284748780-1f386c64a-2606-0266-e053-dadaa90a7c1aMedorrhinum 15C
0220-7310-412023-01-30C16284748780-1f386c64a-2606-0266-e053-dadaa90a7c1aMedorrhinum 15C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-7310-41Medorrhinum15 [hp_C] in 1 TUBEPELLET152

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-7310MEDORRHINUM (GONORRHEAL URETHRAL SECRETION HUMAN ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231116_8631f27c-9a82-edb7-e053-2a91aa0a7978.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-7310-410022073104115 [hp_C] in 1 TUBE (0220-7310-41) 1983-03-030000-00-00NoNoCurrent