Digitalis purpurea
- Product NDC
- 0220-1761
- 11-digit product format
- 002201761
- Labeler code
- 0220
- Product ID
- 0220-1761_f2f3b480-803e-331c-e053-2a95a90a745b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIGITALIS
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- DIGITALIS
- 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
- Digitalis purpurea
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIGITALIS | 200 [kp_C]/200[kp_C] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F1T8QT9U8B |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-1761-41 | Digitalis purpurea | 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 |
|---|
| 0220-1761 | DIGITALIS PURPUREA (DIGITALIS) PELLET [BOIRON] | 2 | Current NDC, Legacy NDC, 1 package rows | 20230124_857b38d7-65fe-3ce2-e053-2a91aa0a7de9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-1761-41 | 00220176141 | 200 [kp_C] in 1 TUBE (0220-1761-41) | 1983-03-03 | 0000-00-00 | No | No | Current |