Vitis Stibium
- Product NDC
- 48951-9158
- 11-digit product format
- 489519158
- Labeler code
- 48951
- Product ID
- 48951-9158_7f0a916b-01b5-7d72-e053-2991aa0a2894
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Vitis Stibium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- FRAGARIA VESCA WHOLE; VITIS VINIFERA LEAF; CALCIUM CATION; ANTIMONY
- Active strength
- 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 48951-9158-4 | 48951915804 | 250 TABLET in 1 BOTTLE, GLASS (48951-9158-4) | 250 tablet | 2009-09-01 | 0000-00-00 | No | No | Current |