Is Cumberland Pharmaceuticals Inc. FDA approved?

Cumberland Pharmaceuticals Inc. holds no registered establishment of its own; 7 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does Cumberland Pharmaceuticals Inc. make?

7 products are listed under Cumberland Pharmaceuticals Inc. in the openFDA NDC Directory, most often as injection; powder, for solution; injection, powder, lyophilized, for solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Are any Cumberland Pharmaceuticals Inc. products in shortage?

1 presentation is currently listed in the FDA drug shortage database under Cumberland Pharmaceuticals Inc., covering Conivaptan Hydrochloride Injection.

Cumberland Pharmaceuticals Inc.

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

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Registered sites: 0
Active NDC listings: 7
Live patents: 0
Shortage listings: 1
Countries: 0

Alert

Drug shortage listings

Drug	Presentation	Status	Availability	Posted / updated
Conivaptan Hydrochloride InjectionCardiovascular	Vaprisol Dextrose In Plastic Container, Injection, 20 mg/100 mL (NDC 66220-160-10)	Current	Unavailable	14 Mar 202216 Sept 2026

Catalogue

Drug listings by form and route

7 active NDC listings: 7 human prescription drug. By marketing category: NDA 5, ANDA 2.

Dosage form	NDCs
injection	2
powder, for solution	2
injection, powder, lyophilized, for solution	1
injection, solution	1
patch	1

Route	NDCs
intravenous	4
oral	2
transdermal	1

Labeller name on the listing	NDCs
cumberland pharmaceuticals inc.	7

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
ACETADOTE	Acetylcysteine	injection, solution, intravenous	66220-207NDA
Caldolor	ibuprofen	injection, intravenous	66220-284NDA
Caldolor	ibuprofen	injection, intravenous	66220-287NDA
KRISTALOSE	lactulose	powder, for solution, oral	66220-719ANDA
KRISTALOSE	lactulose	powder, for solution, oral	66220-729ANDA
SANCUSO	granisetron	patch, transdermal	66220-637NDA
VIBATIV	telavancin hydrochloride	injection, powder, lyophilized, for solution, intravenous	66220-315NDA

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Enquiry

Common questions

Is Cumberland Pharmaceuticals Inc. FDA approved?: Cumberland Pharmaceuticals Inc. holds no registered establishment of its own; 7 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Cumberland Pharmaceuticals Inc. make?: 7 products are listed under Cumberland Pharmaceuticals Inc. in the openFDA NDC Directory, most often as injection; powder, for solution; injection, powder, lyophilized, for solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Are any Cumberland Pharmaceuticals Inc. products in shortage?: 1 presentation is currently listed in the FDA drug shortage database under Cumberland Pharmaceuticals Inc., covering Conivaptan Hydrochloride Injection.

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.