Cinacalcet
- Product NDC
- 71093-152
- 11-digit product format
- 710930152
- Labeler code
- 71093
- Product ID
- 71093-152_09785dc6-18ef-4875-a56a-b4f8ae02e54d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cinacalcet Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ACI Healthcare USA, Inc
- Application
- ANDA213325
- Marketing category
- ANDA
- Marketing start
- 2021-04-01
- Marketing end
- 0000-00-00
- Substance
- CINACALCET HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Calcium-sensing Receptor Agonist [EPC],Increased Calcium-sensing Receptor Sensitivity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71093-152-01 | 71093015201 | 30 TABLET in 1 BOTTLE (71093-152-01) | 30 tablet | 2021-04-01 | 0000-00-00 | No | No | Current |