Folvyris
- Product NDC
- 85477-823
- 11-digit product format
- 854770823
- Labeler code
- 85477
- Product ID
- 85477-823_f1b8c012-47a6-4d0a-a971-97ca8eef4cda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Folate, Vitamin D3
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Oncora Pharma, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-05-01
- Substance
- FOLATE SODIUM; VITAMIN D
- Active strength
- 1.7; .125 mg/1; mg/1
- Pharmacologic classes
- Vitamin D [CS], Vitamin D [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Folvyris
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FOLATE SODIUM | 1.7 mg/1 |
| VITAMIN D | .125 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9P9W8GGU78, 9VU1KI44GP |
| Rxcui | 1720258 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85477-823-30 | Folvyris | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85477-823-30 | 85477082330 | 30 TABLET in 1 BOTTLE (85477-823-30) | 30 tablet | 2026-05-01 | No | No | Historical |