Is Creekwood Pharmaceuticals LLC FDA approved?

Creekwood Pharmaceuticals LLC holds no registered establishment of its own; 38 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does Creekwood Pharmaceuticals LLC make?

38 products are listed under Creekwood Pharmaceuticals LLC in the openFDA NDC Directory, most often as capsule; tablet; capsule, extended release. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Creekwood Pharmaceuticals LLC

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

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Registered sites: 0
Active NDC listings: 38
Live patents: 0
Countries: 0

Catalogue

Drug listings by form and route

38 active NDC listings: 38 human prescription drug. By marketing category: ANDA 38.

Dosage form	NDCs
capsule	21
tablet	13
capsule, extended release	4

Route	NDCs
oral	38

Labeller name on the listing	NDCs
creekwood pharmaceuticals llc	38

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
ATOMOXETINE	atomoxetine	capsule, oral	82619-115ANDA
ATOMOXETINE	atomoxetine	capsule, oral	82619-116ANDA
ATOMOXETINE	atomoxetine	capsule, oral	82619-117ANDA
ATOMOXETINE	atomoxetine	capsule, oral	82619-118ANDA
ATOMOXETINE	atomoxetine	capsule, oral	82619-119ANDA
ATOMOXETINE	atomoxetine	capsule, oral	82619-120ANDA
ATOMOXETINE	atomoxetine	capsule, oral	82619-121ANDA
FENOFIBRATE	fenofibrate	tablet, oral	82619-101ANDA
FENOFIBRATE	fenofibrate	tablet, oral	82619-102ANDA
Gabapentin	Gabapentin	capsule, oral	82619-142ANDA
Gabapentin	Gabapentin	capsule, oral	82619-143ANDA
Gabapentin	Gabapentin	capsule, oral	82619-144ANDA
Gabapentin	Gabapentin	tablet, oral	82619-145ANDA
Gabapentin	Gabapentin	tablet, oral	82619-146ANDA
HALOPERIDOL	haloperidol	tablet, oral	82619-105ANDA
HALOPERIDOL	haloperidol	tablet, oral	82619-106ANDA
HALOPERIDOL	haloperidol	tablet, oral	82619-107ANDA
HALOPERIDOL	haloperidol	tablet, oral	82619-108ANDA
HALOPERIDOL	haloperidol	tablet, oral	82619-109ANDA
HALOPERIDOL	haloperidol	tablet, oral	82619-110ANDA
HYDROXYCHLOROQUINE SULFATE	hydroxychloroquine sulfate	tablet, oral	82619-131ANDA
NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS)	Nitrofurantoin (monohydrate/macrocrystals)	capsule, oral	82619-147ANDA
PREGABALIN	Pregabalin	capsule, oral	82619-122ANDA
PREGABALIN	Pregabalin	capsule, oral	82619-123ANDA
PREGABALIN	Pregabalin	capsule, oral	82619-124ANDA
PREGABALIN	Pregabalin	capsule, oral	82619-125ANDA
PREGABALIN	Pregabalin	capsule, oral	82619-126ANDA
PREGABALIN	Pregabalin	capsule, oral	82619-127ANDA
PREGABALIN	Pregabalin	capsule, oral	82619-128ANDA
PREGABALIN	Pregabalin	capsule, oral	82619-129ANDA
Propranolol Hydrochloride	Propranolol Hydrochloride	capsule, extended release, oral	82619-132ANDA
Propranolol Hydrochloride	Propranolol Hydrochloride	capsule, extended release, oral	82619-133ANDA
Propranolol Hydrochloride	Propranolol Hydrochloride	capsule, extended release, oral	82619-134ANDA
Propranolol Hydrochloride	Propranolol Hydrochloride	capsule, extended release, oral	82619-135ANDA
RIZATRIPTAN BENZOATE	rizatriptan benzoate	tablet, oral	82619-111ANDA
RIZATRIPTAN BENZOATE	rizatriptan benzoate	tablet, oral	82619-112ANDA
SILODOSIN	silodosin	capsule, oral	82619-113ANDA
SILODOSIN	silodosin	capsule, oral	82619-114ANDA

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Enquiry

Common questions

Is Creekwood Pharmaceuticals LLC FDA approved?: Creekwood Pharmaceuticals LLC holds no registered establishment of its own; 38 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Creekwood Pharmaceuticals LLC make?: 38 products are listed under Creekwood Pharmaceuticals LLC in the openFDA NDC Directory, most often as capsule; tablet; capsule, extended release. 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.