Revesta
- Product NDC
- 69336-330
- 11-digit product format
- 693360330
- Labeler code
- 69336
- Product ID
- 69336-330_99d751a9-5482-0c33-e053-2a95a90a1d82
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Revesta
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sterling Knight Pharmaceuticals,LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2016-10-13
- Marketing end
- 0000-00-00
- Substance
- CHOLECALCIFEROL; FOLIC ACID
- Active strength
- 5750 [iU]/1; mg/1
- Pharmacologic classes
- Vitamin D [CS],Vitamin D [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69336-330-30 | Revesta | 30 in 1 BOTTLE, PLASTIC | CAPSULE | 30 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69336-330 | REVESTA CAPSULE [STERLING KNIGHT PHARMACEUTICALS,LLC] | 9 | Legacy NDC, 1 package rows | 20191217_e5567a73-bf94-4bad-ade6-ddef18c8af04.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69336-330-30 | 69336033030 | 30 in 1 BOTTLE, PLASTIC | Historical |