MYQORZO
- Product NDC
- 82112-105
- 11-digit product format
- 821120105
- Labeler code
- 82112
- Product ID
- 82112-105_f48908e6-f578-4e6c-b4ac-d4af4f01fdd6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AFICAMTEN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cytokinetics Inc.
- Application
- NDA219083
- Marketing category
- NDA
- Marketing start
- 2026-01-12
- Substance
- AFICAMTEN
- Active strength
- 5 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MYQORZO
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AFICAMTEN | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | B1I77MH6K1 |
| Rxcui | 2731474, 2731480, 2731482, 2731484, 2731486, 2731488, 2731490, 2731492 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82112-105-30 | MYQORZO | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 2 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 82112-105-30 | 82112010530 | 30 TABLET, FILM COATED in 1 BOTTLE (82112-105-30) | 2026-01-12 | No | No | Historical |