BM Ruta Graveolens
- Product NDC
- 85816-5088
- Requested package NDC
- 85816-5088-1
- 11-digit product format
- 858165088
- Labeler code
- 85816
- Product ID
- 85816-5088_5ebf8286-c37e-e330-e063-6394a90a2e3d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ruta Graveolens
- Dosage form
- GLOBULE
- Route
- ORAL
- Labeler
- BM Private Limited
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-01
- Substance
- RUTA GRAVEOLENS FLOWERING TOP
- Active strength
- 200 [hp_C]/1000mg
- 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 Ruta Graveolens
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| RUTA GRAVEOLENS FLOWERING TOP | 200 [hp_C]/1000mg |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85816-5088-1 | BM Ruta Graveolens | 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 |
|---|
| 85816-5088-1 | 85816508801 | 30000 mg in 1 BOTTLE, GLASS (85816-5088-1) | 30000 mg | 2015-01-01 | No | No | Current |