BM Digitalis Purpurea
- Product NDC
- 85816-5106
- 11-digit product format
- 858165106
- Labeler code
- 85816
- Product ID
- 85816-5106_38dfb441-b08b-b6a8-e063-6394a90a72ef
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Digitalis Purpurea
- Dosage form
- GLOBULE
- Route
- ORAL
- Labeler
- BM Private Limited
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-01
- Substance
- DIGITALIS
- Active strength
- 30 [hp_C]/1000mg
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BM Digitalis Purpurea
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIGITALIS | 30 [hp_C]/1000mg |
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 |
|---|
| 85816-5106-1 | BM Digitalis Purpurea | 30000 mg in 1 BOTTLE, GLASS | GLOBULE | 30000 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85816-5106-1 | 85816510601 | 30000 mg in 1 BOTTLE, GLASS (85816-5106-1) | 30000 mg | 2015-01-01 | No | No | Historical |