NDC 59088-768 - Nuvazil II

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 59088-768
Package NDCs from labels: 59088-768-90
Manufacturer: PureTek Corporation
Effective date: 2021-02-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Nuvazil II - PureTek Corporation	PureTek Corporation	2021-02-08	MEDICAL DEVICE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59088-768-90	Nuvazil II	1 in 1 POUCH		1		2
59088-768-90	Nuvazil II	4 in 1 POUCH		4		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59088-768	NUVAZIL II () [PURETEK CORPORATION]	2	2 package rows	20210209_fcec585c-7f57-4e2e-8239-8bda5a8648c7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59088-768-90	EA - Each	59088-768	7d99a7bd-ada5-42a5-aaa4-7435d4b37e7e	1	2021-02-05

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 9 of 9 · 169 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Lydexa 4.12%	LIDOCAINE HYDROCHLORIDE	PureTek Corporation	aa1c9d39-1283-8c6b-e053-2a95a90af5b5	2022-03-02	Warnings, Adverse reactions	Name fallback manufacturer name: PureTek Corporation
Micomitin Antifungal	CLOTRIMAZOLE	PureTek Corporation	dd05f5f9-2412-1295-e053-2995a90acb96	2022-02-14	Warnings	Name fallback manufacturer name: PureTek Corporation
Dotremin	FOLIC ACID, VITAMIN D3	PureTek Corporation	cd132db2-7ff7-a9eb-e053-2995a90a02c5	2022-01-14	Warnings, Adverse reactions	Name fallback manufacturer name: PureTek Corporation
Gaba 300-EZS	GABAPENTIN	PureTek Corporation	bb29692e-1546-4d05-a46a-93baf4172c7d	2020-11-16	Warnings, Adverse reactions	Name fallback manufacturer name: PureTek Corporation
Lidoxryl	LIDOCAINE	PureTek Corporation	1c33790b-8d57-46e8-bd6e-5a0f87a3c29f	2020-11-10	Warnings, Adverse reactions	Name fallback manufacturer name: PureTek Corporation
Methocarb 500-EZS	METHOCARBAMOL	PureTek Corporation	383ce408-1085-43e7-944e-957ff2a9d553	2020-11-10	Warnings, Adverse reactions	Name fallback manufacturer name: PureTek Corporation
LidoPure Patch	LIDOCAINE	PureTek Corporation	c851c6e9-1966-4639-9406-fe6adc91c9d0	2020-11-10	Warnings, Adverse reactions	Name fallback manufacturer name: PureTek Corporation
Foltrexyl	FOLIC ACID, VITAMIN D3	PureTek Corporation	b2d71f92-018f-183e-e053-2995a90a5db0	2020-10-29	Warnings, Adverse reactions	Name fallback manufacturer name: PureTek Corporation
DermacinRx Lidotral	LIDOCAINE HYDROCHLORIDE	PureTek Corporation	23efec58-67cc-418d-85f5-7ef156443cbf	2019-02-04	Warnings, Adverse reactions	Name fallback manufacturer name: PureTek Corporation

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.