Helleborus comp. A
- Product NDC
- 48951-5116
- 11-digit product format
- 489515116
- Labeler code
- 48951
- Product ID
- 48951-5116_8f6095fa-471a-6b31-e053-2a95a90a09c7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Helleborus comp. A
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- LEAD MONOSILICATE; FORMICA RUFA; SILVER; ANTIMONY; PHOSPHORUS; HELLEBORUS NIGER ROOT; ARSENIC TRIOXIDE
- Active strength
- 20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- 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 |
|---|
| 48951-5116-1 | 48951511601 | 10 AMPULE in 1 BOX (48951-5116-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |