Vitis Stibium
- Product NDC
- 48951-9360
- 11-digit product format
- 489519360
- Labeler code
- 48951
- Product ID
- 48951-9360_c10e6dbb-9b4f-9bef-e053-2a95a90a57ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Vitis Stibium
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2021-04-27
- Marketing end
- 0000-00-00
- Substance
- FRAGARIA VESCA WHOLE; CALCIUM CATION; VITIS VINIFERA LEAF; ANTIMONY
- Active strength
- 1 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-9360-7 | 48951936007 | 75 g in 1 BOTTLE (48951-9360-7) | 75 g | 2021-04-27 | 0000-00-00 | No | No | Current |