Opium 30C

Product NDC
69152-1111
11-digit product format
691521111
Labeler code
69152
Product ID
69152-1111_1916d2e3-16ba-0ac0-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Opium
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2017-05-11
Marketing end
0000-00-00
Substance
OPIUM
Active strength
30 [hp_C]/1
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
69152-1111-12020-01-31C16284748780-19d75b9d0-292c-f424-e053-dadaa90a57ce1916d2e3-16b9-0ac0-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1111-1Opium 30C96 in 1 BOTTLEPELLET961

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1111OPIUM 30C (OPIUM) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]1Legacy NDC, 1 package rows20170513_1916d2e3-16b9-0ac0-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1111-16915211110196 in 1 BOTTLEHistorical