Drug

Who makes clotrimazole and betamethasone dipropionate?

15 companies list clotrimazole and betamethasone dipropionate as a human prescription drug. Forms: cream; lotion. Routes: topical.

Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology

Companies listing clotrimazole and betamethasone dipropionate

CompanyFormsApplicationNDCsRegistered sites
International Medication Systems, Ltd.United StatescreamANDAANDA075673, ANDA07600243
Sun Pharmaceutical Industries LimitedIndiacream; lotionANDAANDA075673, ANDA076493213
Proficient Rx LPUnited StatescreamANDAANDA076002, ANDA20289421
Glenmark Pharmaceuticals Inc., USAIndiacreamANDAANDA20289419
ADVANCED RX PHARMACY OF TENNESSEE LLCUnited StatescreamANDAANDA07567311
Actavis LLCUnited StatescreamANDAANDA07600211
Bryant Ranch PrepackUnited StatescreamANDAANDA07600211
Direct RxUnited StatescreamANDAANDA20289411
NuCare Pharmaceuticals,Inc.United StatescreamANDAANDA20289411
Preferred Pharmaceuticals Inc.United StatescreamANDAANDA07567311
RedPharm DrugUnited StatescreamANDAANDA07567311
RemedyRepack, IncUnited StatescreamANDAANDA07567311
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLCcreamANDAANDA07550210
Northstar Rx, LLC,creamANDAANDA07567310
Sportpharm LLCcreamANDAANDA07567310
Enquiry

Common questions

Who makes clotrimazole and betamethasone dipropionate?
15 companies list clotrimazole and betamethasone dipropionate as a human prescription drug in the openFDA NDC Directory, led by International Medication Systems, Ltd., Sun Pharmaceutical Industries Limited, Proficient Rx LP, Glenmark Pharmaceuticals Inc., USA, ADVANCED RX PHARMACY OF TENNESSEE LLC. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
Is there a generic clotrimazole and betamethasone dipropionate?
15 companies list clotrimazole and betamethasone dipropionate under an abbreviated new drug application (ANDA), the application type used for generics. Listing status is from the NDC Directory; it is not a statement of availability.