Cantharis
- Product NDC
- 0220-1111
- 11-digit product format
- 002201111
- Labeler code
- 0220
- Product ID
- 0220-1111_003a6ff4-44c7-0cb3-e063-6294a90a6f4a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- LYTTA VESICATORIA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- LYTTA VESICATORIA
- Active strength
- 200 [kp_C]/200[kp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cantharis
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LYTTA VESICATORIA | 200 [kp_C]/200[kp_C] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3Q034RO3BT |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-1111-41 | Cantharis | 200 [kp_C] in 1 TUBE | PELLET | 200 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-1111 | CANTHARIS (LYTTA VESICATORIA ) PELLET [BOIRON] | 2 | Current NDC, Legacy NDC, 1 package rows | 20230712_851544d1-6816-736d-e053-2a91aa0ae02d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-1111-41 | 00220111141 | 200 [kp_C] in 1 TUBE (0220-1111-41) | 1983-03-03 | 0000-00-00 | No | No | Current |