Cinacalcet
- Product NDC
- 63629-8764
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cinacalcet
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210570
- Marketing category
- ANDA
- Substance
- CINACALCET HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 63629-8764-1 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-8764-1) | 20190518 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| c288922b-3258-4c1c-bd8a-32a41dd43a63 | These highlights do not include all the information needed to use CINACALCET TABLETS safely and effectively. See full prescribing information for CINACALCET TABLETS. CINACALCET tablets , for oral use Initial U.S. Approval: 2004 | Bryant Ranch Prepack | 2023-10-30 | HUMAN PRESCRIPTION DRUG LABEL | 105 |