Osteodoron PM Special Formula
- Product NDC
- 48951-7161
- Requested package NDC
- 48951-7161-4
- 11-digit product format
- 489517161
- Labeler code
- 48951
- Product ID
- 48951-7161_6bb1d864-6349-6b0c-e053-2991aa0ab4c9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Osteodoron PM Special Formula
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- CALCIUM FLUORIDE; SILICON DIOXIDE; LEAD CARBONATE; OSTREA EDULIS SHELL; QUERCUS ROBUR WHOLE
- Active strength
- 6 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-7161-4 | Osteodoron PM Special Formula | 50 g in 1 BOTTLE, GLASS | POWDER | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-7161 | OSTEODORON PM SPECIAL FORMULA POWDER [URIEL PHARMACY INC.] | 2 | Legacy NDC, 1 package rows | 20240118_6bb1d864-6348-6b0c-e053-2991aa0ab4c9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-7161-4 | 48951716104 | 50 g in 1 BOTTLE, GLASS (48951-7161-4) | 50 g | 2009-09-01 | 0000-00-00 | No | No | Current |