Anacardium

Product NDC: 53645-1870
11-digit product format: 536451870
Labeler code: 53645
Product ID: 53645-1870_9a3a6a5b-b7b5-7cc3-e053-2a95a90a4b76
Type: HUMAN OTC DRUG
Nonproprietary name: Anacardium
Dosage form: GLOBULE
Route: ORAL
Labeler: True Botanica, LLC
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2014-02-03
Marketing end: 0000-00-00
Substance: STRYCHNOS NUX-VOMICA SEED
Active strength: 30 [hp_X]/23g
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53645-1870-3	2025-12-09	C162847	48780-1	ba0f9c33-16bf-a910-e053-dadaa90a0b85	6195d0f8-27b9-7c1e-e053-2991aa0a7b1a
53645-1870-3	2021-01-29	C162847	48780-1	ba0f9c33-16bf-a910-e053-dadaa90a0b85	6195d0f8-27b9-7c1e-e053-2991aa0a7b1a

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53645-1870	ANACARDIUM GLOBULE [TRUE BOTANICA, LLC]	2	Legacy NDC	20191222_6195d0f8-27b9-7c1e-e053-2991aa0a7b1a.zip