Osteodoron AM Bone Support
- Product NDC
- 48951-7096
- 11-digit product format
- 489517096
- Labeler code
- 48951
- Product ID
- 48951-7096_009d1de0-2bc6-11df-8a39-0800200c9a66
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PUMPKIN SILICON DIOXIDE CALCIUM FLUORIDE FLUORAPATITE
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- PUMPKIN; SILICON DIOXIDE; CALCIUM FLUORIDE; FLUORAPATITE
- Active strength
- 3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-7096-4 | Osteodoron AM Bone Support | 1 in 1 BOTTLE, GLASS | POWDER | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-7096 | OSTEODORON AM BONE SUPPORT (PUMPKIN SILICON DIOXIDE CALCIUM FLUORIDE FLUORAPATITE) POWDER [URIEL PHARMACY INC] | 1 | Legacy NDC, 1 package rows | 20100312_1dfca5e0-2bc6-11df-8a39-0800200c9a66.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 48951-7096-4 | 48951709604 | 1 in 1 BOTTLE, GLASS | Historical |