Fucus Vesiculosus
- Product NDC
- 57520-0676
- 11-digit product format
- 575200676
- Labeler code
- 57520
- Product ID
- 57520-0676_084614ed-3ecc-4225-9b10-53836cdcf8f9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Fucus vesiculosus,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Apotheca Company
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-04-11
- Marketing end
- 2022-09-21
- Substance
- FUCUS VESICULOSUS
- Active strength
- 30 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57520-0676-1 | 57520067601 | 30 mL in 1 BOTTLE, DROPPER (57520-0676-1) | 30 ml | 2011-04-11 | 2022-09-21 | No | No | Current |