BM Belladonna
- Product NDC
- 85816-5022
- 11-digit product format
- 858165022
- Labeler code
- 85816
- Product ID
- 85816-5022_5c55a74d-2235-8f1b-e063-6394a90a2a47
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Belladonna
- Dosage form
- GLOBULE
- Route
- ORAL
- Labeler
- BM Private Limited
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-01
- Substance
- ATROPA BELLADONNA
- Active strength
- 30 [hp_C]/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BM Belladonna
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ATROPA BELLADONNA | 30 [hp_C]/g |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85816-5022-1 | BM Belladonna | 30 g in 1 BOTTLE, GLASS | GLOBULE | 30 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85816-5022-1 | 85816502201 | 30 g in 1 BOTTLE, GLASS (85816-5022-1) | 30 g | 2015-01-01 | No | No | Current |