Medorrhinum

Product NDC
0220-7311
11-digit product format
002207311
Labeler code
0220
Product ID
0220-7311_0a35f0c9-696a-e38a-e063-6294a90afb5c
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
30 [hp_C]/30[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 HUMAN30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9BZG9E3I8F

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-7311-412023-11-15C16284748780-1f386c649-bc77-0266-e053-dadaa90a7c1aMedorrhinum 30C
0220-7311-412023-01-30C16284748780-1f386c649-bc77-0266-e053-dadaa90a7c1aMedorrhinum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-7311-41Medorrhinum30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-7311MEDORRHINUM (GONORRHEAL URETHRAL SECRETION HUMAN ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231116_86320c87-6f4b-548c-e053-2a91aa0a8c00.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-7311-410022073114130 [hp_C] in 1 TUBE (0220-7311-41) 1983-03-030000-00-00NoNoCurrent