Pertussinum

Product NDC
55714-9011
11-digit product format
557149011
Labeler code
55714
Product ID
55714-9011_0a0cf5e8-378f-99bc-e063-6294a90a1694
Type
HUMAN OTC DRUG
Nonproprietary name
Pertussinum
Dosage form
LIQUID
Route
ORAL
Labeler
Newton Laboratories, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-01-01
Substance
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED
Active strength
30 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55714-9011-12023-11-13C16284748780-1d6a99b39-5291-a426-e053-dadaa90af4c2Pertussinum 9011L
55714-9011-12022-01-28C16284748780-1d6a99b39-5291-a426-e053-dadaa90af4c2Pertussinum 9011L

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55714-9011-1Pertussinum30 mL in 1 BOTTLE, GLASSLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55714-9011PERTUSSINUM LIQUID [NEWTON LABORATORIES, INC.]2Current NDC, Legacy NDC, 1 package rows20231114_9e3c2059-4e58-54b2-e053-2a95a90a24f6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55714-9011-15571490110130 mL in 1 BOTTLE, GLASS (55714-9011-1) 30 ml2020-01-010000-00-00NoNoCurrent