NDC 62327-333-03 - Steritalc 4g

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: 62327-333
Requested NDC: 62327-333-03
Package NDCs from labels: 62327-333-03, 62327-333-43
Manufacturer: Novatech SA
Effective date: 2025-06-25
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Steritalc 4g - Novatech SA	Novatech SA	2025-06-25	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62327-333-03	Steritalc3g	10 mL in 1 VIAL, GLASS	POWDER	10		7
62327-333-43	Steritalc3g	4 in 1 BOX	POWDER	4		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62327-333	STERITALC 4G (TALC) POWDER STERITALC 2G (TALC) POWDER STERITALC 3G (TALC) POWDER [NOVATECH SA]	5	Current NDC, Legacy NDC, 2 package rows	20250508_c94e51d9-beef-4b06-e053-2a95a90a754a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
62327-333-03	EA - Each	62327-333	21af2c8d-7a9d-485a-bd19-285c45dc7484	1	2021-09-07
62327-333-43	EA - Each	62327-333	393d8a1c-da00-4f07-bf82-f14a3e239a95	1	2021-09-07

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 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Steritalc 2g	TALC	Novatech SA	c94e51d9-beef-4b06-e053-2a95a90a754a	2025-06-25	Warnings, Adverse reactions	Exact identifier application number: NDA205555 ndc (package): 62327-333-03 ndc (package): 62327-444-04 ndc (package): 62327-222-02 ndc (package): 62327-444-44 ndc (package): 62327-333-43 ndc (package): 62327-222-42 ndc (product): 62327-333 ndc (product): 62327-222 ndc (product): 62327-444 ndc11 (package): 62327033303 rxcui: 2003393 rxcui: 2003405 rxcui: 2003402 rxcui: 2003403 rxcui: 2003400 rxcui: 2003398 spl id: 386130d4-1b0d-5e87-e063-6394a90aefa7 spl set id: c94e51d9-beef-4b06-e053-2a95a90a754a unii: 7SEV7J4R1U
SENSITIVE POCKET SUN	SENSITIVE POCKET SUN	Shantou Oushiya Biotechnology Co., Ltd	36ac412f-e31f-6906-e063-6394a90a4a3d	2025-06-14	Warnings	Exact identifier unii: 7SEV7J4R1U

Reported adverse events (FAERS/openFDA)#

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