ZENTEL

Product NDC: 72689-0036
11-digit product format: 726890036
Labeler code: 72689
Product ID: 72689-0036_8468a205-d3bb-4ed5-e053-2a91aa0a9122
Type: HUMAN OTC DRUG
Nonproprietary name: Albendazole
Dosage form: TABLET
Route: ORAL
Labeler: OASIS TRADING
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2018-11-15
Marketing end: 0000-00-00
Substance: ALBENDAZOLE
Active strength: 400 mg/1
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
b0e27303-91cd-2fd1-e9ec-fbe22a3c3f49	Product name	8	20250325

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72689-0036-1	2021-01-29	C162847	48780-1	ba0f9c33-2fbb-a910-e053-dadaa90a0b85	8469156a-6aae-42cd-e053-2a91aa0a10ba

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72689-0036-1	ZENTEL	2 in 1 BLISTER PACK	TABLET	2		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72689-0036	ZENTEL (ALBENDAZOLE) TABLET [OASIS TRADING]	1	Legacy NDC, 1 package rows	20190319_8469156a-6aae-42cd-e053-2a91aa0a10ba.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Status
72689-0036-1	72689003601	2 in 1 BLISTER PACK	Historical