Prevent Restoration
- Product NDC
- 55259-9001
- 11-digit product format
- 552599001
- Labeler code
- 55259
- Product ID
- 55259-9001_aeabd1de-fe6a-dce9-e053-2995a90a0472
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- oyster shell
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- APEXEL CO., LTD.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-09-07
- Marketing end
- 0000-00-00
- Substance
- OSTREA EDULIS SHELL
- Active strength
- 1 1/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 55259-9001-1 | Prevent Restoration | 120 in 1 BOTTLE | TABLET | 120 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55259-9001 | PREVENT RESTORATION (OYSTER SHELL) TABLET [APEXEL CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20200907_aeabd181-184a-913d-e053-2a95a90ae3ae.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55259-9001-1 | 55259900101 | 120 TABLET in 1 BOTTLE (55259-9001-1) | 120 tablet | 2020-09-07 | 0000-00-00 | No | No | Current |