Ammonium carbonicum 200C

Product NDC
69152-1053
11-digit product format
691521053
Labeler code
69152
Product ID
69152-1053_2f2e2220-6fbb-0e0a-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Ammonium carbonicum
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-06-15
Marketing end
0000-00-00
Substance
AMMONIUM CARBONATE
Active strength
200 [hp_C]/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1053-12020-01-31C16284748780-19d75b9d0-7867-f424-e053-dadaa90a57ce1888f734-c36f-3bf4-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1053-1Ammonium carbonicum 200C96 in 1 BOTTLEPELLET963

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1053AMMONIUM CARBONICUM 200C (AMMONIUM CARBONICUM) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]3Legacy NDC, 1 package rows20160329_1888f734-c36f-3bf4-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1053-16915210530196 in 1 BOTTLEHistorical