Drug company (FDA labeler)
CMP Pharma, Inc.
NDC labeler code: 46287
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- Sodium polystyrene sulfonateKionex · 2 products
- AmlodipineNorvasc, Sdamlo, Norliqva · 2 products
- TadalafilCialis, Tadliq, Adcirca · 1 product
- ClonidineClonidine Transdermal System, Catapres-Tts-1, Clonidine Transdermal System Usp, 0.1 Mg/Day · 1 product
- Isoniazid1 product
- Triamcinolone acetonideKenalog-40, Triderm, Triesence · 1 product
- SpironolactoneAldactone · 1 product
- AtorvastatinLipitor · 1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| July 29, 2026 | NDA221094 | Clonidine QLONILIK | Cmp Dev LLC |
| February 1, 2023 | NDA213260 | Atorvastatin ATORVALIQ | Cmp Dev LLC |
| June 17, 2022 | NDA214522 | Tadalafil TADLIQ | Cmp Dev LLC |
| February 24, 2022 | NDA214439 | Amlodipine NORLIQVA | Cmp Dev LLC |
| August 4, 2017 | NDA209478 | Spironolactone CAROSPIR | Cmp Dev LLC |
| March 23, 1995 | ANDA089595 | Triamcinolone acetonide TRIANEX | Pharmobedient |
| January 19, 1989 | ANDA089910 | Sodium polystyrene sulfonate SODIUM POLYSTYRENE SULFONATE | Cmp Pharma Inc |
| November 10, 1983 | ANDA088235 | Isoniazid ISONIAZID | Cmp Pharma Inc |
| December 8, 1982 | ANDA087859 | Sodium polystyrene sulfonate SPS | Cmp Pharma Inc |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026