Vitis Stibium
- Product NDC
- 48951-9367
- 11-digit product format
- 489519367
- Labeler code
- 48951
- Product ID
- 48951-9367_ed730437-f719-4bd2-e053-2a95a90af6b4
- 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
- ANTIMONY; CALCIUM FORMATE; FRAGARIA VESCA WHOLE; VITIS VINIFERA LEAF
- Active strength
- 5 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- Pharmacologic classes
- Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 48951-9367-4 | 48951936704 | 50 TABLET in 1 BOTTLE, GLASS (48951-9367-4) | 50 tablet | 2009-09-01 | 0000-00-00 | No | No | Current |