Is GRANULATION TECHNOLOGY, INC. FDA approved?

GRANULATION TECHNOLOGY, INC. 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 GRANULATION TECHNOLOGY, INC.'s drugs manufactured?

The FDA register lists FAIRFIELD, NJ. Registered operations: finished drug manufacture.

What drugs does GRANULATION TECHNOLOGY, INC. make?

16 products are listed under GRANULATION TECHNOLOGY, INC. in the openFDA NDC Directory, most often as tablet; tablet, film coated; powder, for solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

GRANULATION TECHNOLOGY, INC.

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

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Registered sites: 1
Active NDC listings: 16
Live patents: 0
Countries: 1
Base: United States

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
GRANULATION TECHNOLOGY, INC.	12 Industrial Road, FAIRFIELD, New Jersey (NJ) 07004, United States (USA)	Finished drug manufacture	3001236066847132193

Catalogue

Drug listings by form and route

16 active NDC listings: 12 human prescription drug, 4 human otc drug. By marketing category: ANDA 6, OTC MONOGRAPH DRUG 4, NDA 3, UNAPPROVED DRUG OTHER 3.

Dosage form	NDCs
tablet	9
tablet, film coated	5
powder, for solution	1
tablet, orally disintegrating	1

Route	NDCs
oral	14
sublingual	1
topical	1

Labeller name on the listing	NDCs
granulation technology, inc.	16

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Astringent	Calcium acetate monohydrate and Aluminum sulfate tetradecahydrate	powder, for solution, topical	63561-0178OTC MONOGRAPH DRUG
Carisoprodol Tablets, USP, 350 mg	Carisoprodol	tablet, oral	63561-0127ANDA
Furosemide	FUROSEMIDE	tablet, oral	63561-0164NDA
Furosemide	FUROSEMIDE	tablet, oral	63561-0165NDA
Furosemide	FUROSEMIDE	tablet, oral	63561-0166NDA
Hyoscyamine Sulfate	Hyoscyamine Sulfate	tablet, orally disintegrating, oral	63561-0197UNAPPROVED DRUG OTHER
Hyoscyamine Sulfate	Hyoscyamine Sulfate	tablet, sublingual	63561-0202UNAPPROVED DRUG OTHER
Hyoscyamine Sulfate	Hyoscyamine Sulfate	tablet, oral	63561-0203UNAPPROVED DRUG OTHER
Laxative	Sennosides, 25 mg	tablet, film coated, oral	63561-0186OTC MONOGRAPH DRUG
Methocarbamol Tablets, USP, 500 mg	Methocarbamol	tablet, film coated, oral	63561-0173ANDA
Methocarbamol Tablets, USP, 750 mg	Methocarbamol	tablet, film coated, oral	63561-0174ANDA
PredniSONE Tablets, USP, 10 mg	PredniSONE	tablet, oral	63561-0121ANDA
PredniSONE Tablets, USP, 20 mg	PredniSONE	tablet, oral	63561-0122ANDA
PredniSONE Tablets, USP, 5 mg	PredniSONE	tablet, oral	63561-0120ANDA
Senna-S	DOCUSATE SODIUM, SENNOSIDES	tablet, film coated, oral	63561-0187OTC MONOGRAPH DRUG
Vegetable Laxative	SENNOSIDES, 8.6 mg	tablet, film coated, oral	63561-0188OTC MONOGRAPH DRUG

Neighbours

Registered in the same town

SGS North America Inc.Fairfield, NJ
Teva Pharmaceutical Industries Ltd.Fairfield, NJ
API Solutions Inc.Fairfield, NJ
Aarkish Pharmaceuticals NJ IncFairfield, NJ
Akron Pharma Inc.Fairfield, NJ
Garonit Pharmaceutical, Inc.Fairfield, NJ
Leading Pharma, LLCFairfield, NJ

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Enquiry

Common questions

Is GRANULATION TECHNOLOGY, INC. FDA approved?: GRANULATION TECHNOLOGY, INC. 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 GRANULATION TECHNOLOGY, INC.'s drugs manufactured?: The FDA register lists FAIRFIELD, NJ. Registered operations: finished drug manufacture.
What drugs does GRANULATION TECHNOLOGY, INC. make?: 16 products are listed under GRANULATION TECHNOLOGY, INC. in the openFDA NDC Directory, most often as tablet; tablet, film coated; powder, for solution. 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.