Is S&B Pharma LLC dba Norac Pharma FDA approved?

S&B Pharma LLC dba Norac Pharma holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are S&B Pharma LLC dba Norac Pharma's drugs manufactured?

The FDA register lists Azusa, CA. Registered operations: analytical testing, active ingredient (API) manufacture.

What drugs does S&B Pharma LLC dba Norac Pharma make?

7 products are listed under S&B Pharma LLC dba Norac Pharma in the openFDA NDC Directory, most often as powder; liquid. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

S&B Pharma LLC dba Norac Pharma

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 7
Live patents: 0
Countries: 1
Base: United States

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
S&B Pharma LLC dba Norac Pharma	405 South Motor Avenue, Azusa, California (CA) 91702, United States (USA)	Analytical testing, Active ingredient (API) manufacture	2015729117750912

Catalogue

Drug listings by form and route

7 active NDC listings: 7 bulk ingredient. By marketing category: BULK INGREDIENT 7.

Dosage form	NDCs
powder	6
liquid	1

Route	NDCs

Labeller name on the listing	NDCs
s&b pharma llc dba norac pharma	7

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Dexmethylphenidate Hydrochloride	powder	53834-201BULK INGREDIENT
-	Dronabinol	liquid	53834-001BULK INGREDIENT
-	Lisdexamfetamine Dimesylate	powder	53834-401BULK INGREDIENT
-	Methylphenidate Hydrochloride	powder	53834-502BULK INGREDIENT
-	Methylphenidate Hydrochloride	powder	53834-504BULK INGREDIENT
-	Pentobarbital Sodium	powder	53834-601BULK INGREDIENT
-	Tapentadol Hydrochloride	powder	53834-701BULK INGREDIENT

Neighbours

Registered in the same town

Westwood Laboratories, LLC.Azusa, CA

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Enquiry

Common questions

Is S&B Pharma LLC dba Norac Pharma FDA approved?: S&B Pharma LLC dba Norac Pharma holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are S&B Pharma LLC dba Norac Pharma's drugs manufactured?: The FDA register lists Azusa, CA. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does S&B Pharma LLC dba Norac Pharma make?: 7 products are listed under S&B Pharma LLC dba Norac Pharma in the openFDA NDC Directory, most often as powder; liquid. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.