AG-X
- Product NDC
- 55259-8001
- 11-digit product format
- 552598001
- Labeler code
- 55259
- Product ID
- 55259-8001_8f1f0c89-dd2d-2b3a-e053-2a95a90acf3a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- calcium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- APEXEL CO., LTD.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-08-02
- Marketing end
- 0000-00-00
- Substance
- CALCIUM
- Active strength
- 1 1/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55259-8001-1 | AG-X | 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 |
|---|
| 55259-8001 | AG-X (CALCIUM) TABLET [APEXEL CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20190802_8f1f0c89-dd2c-2b3a-e053-2a95a90acf3a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55259-8001-1 | 55259800101 | 120 in 1 BOTTLE | Historical |