Emvita 7
- Product NDC
- 66343-056
- Requested package NDC
- 66343-056-50
- 11-digit product format
- 663430056
- Labeler code
- 66343
- Product ID
- 66343-056_b96efd18-f3fb-1ddb-e053-2a95a90a3e71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anacard occ, Lachesis mutus, Phosphorus, Glandula sup, Lycopodium
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- RUBIMED AG
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-06-03
- Marketing end
- 0000-00-00
- Substance
- ANACARDIUM OCCIDENTALE FRUIT; LACHESIS MUTA VENOM; PHOSPHORUS; SUS SCROFA ADRENAL GLAND; LYCOPODIUM CLAVATUM SPORE
- Active strength
- 18 [hp_M]/50mL; [hp_C]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_M]/50mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 66343-056 | 66343-056-50 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 66343-056-50 | 66343005650 | 50 mL in 1 BOTTLE (66343-056-50) | 50 ml | 2019-06-03 | 0000-00-00 | No | No | Current |