77598-123 NDC - SIMIKA ()

Drug Information

Product NDC: 77598-123

Proprietary Name: SIMIKA

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Guangzhou Ouzhuang Biological Technology Co Ltd
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	5/15/2020

No.	Package Code	Package Description
1	77598-123-01	30 mL in 1 BOTTLE (77598-123-01)
2	77598-123-02	50 mL in 1 BOTTLE (77598-123-02)
3	77598-123-03	60 mL in 1 BOTTLE (77598-123-03)
4	77598-123-04	80 mL in 1 BOTTLE (77598-123-04)
5	77598-123-05	100 mL in 1 BOTTLE (77598-123-05)
6	77598-123-06	200 mL in 1 BOTTLE (77598-123-06)
7	77598-123-07	250 mL in 1 BOTTLE (77598-123-07)
8	77598-123-08	300 mL in 1 BOTTLE (77598-123-08)
9	77598-123-09	500 mL in 1 BOTTLE (77598-123-09)
10	77598-123-10	1000 mL in 1 BOTTLE (77598-123-10)
11	77598-123-11	3000 mL in 1 BOTTLE (77598-123-11)
12	77598-123-12	5000 mL in 1 BOTTLE (77598-123-12)
13	77598-123-20	60 mL in 1 TUBE (77598-123-20)

Field Name	Field Value	Definition
PRODUCT NDC	77598-123	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	SIMIKA	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	5/15/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Guangzhou Ouzhuang Biological Technology Co Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023