Pulsatilla
- Product NDC
- 0220-4194
- 11-digit product format
- 002204194
- Labeler code
- 0220
- Product ID
- 0220-4194_f70744a9-6d8b-4143-e053-6294a90a7b05
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ANEMONE PULSATILLA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- ANEMONE PULSATILLA
- Active strength
- 10 [hp_M]/10[hp_M]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pulsatilla
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANEMONE PULSATILLA | 10 [hp_M]/10[hp_M] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I76KB35JEV |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-4194-41 | Pulsatilla | 10 [hp_M] in 1 TUBE | PELLET | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-4194 | PULSATILLA (ANEMONE PULSATILLA ) PELLET [BOIRON] | 2 | Current NDC, Legacy NDC, 1 package rows | 20230317_86a8ba2f-b9be-3f96-e053-2a91aa0ad64e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-4194-41 | 00220419441 | 10 [hp_M] in 1 TUBE (0220-4194-41) | 1983-03-03 | 0000-00-00 | No | No | Current |