Ruta Graveolens
- Product NDC
- 37662-2269
- 11-digit product format
- 376622269
- Labeler code
- 37662
- Product ID
- 37662-2269_f1a3bd93-80d5-be37-e053-2a95a90a3fd9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ruta Graveolens
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Hahnemann Laboratories, INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-01-06
- Substance
- RUTA GRAVEOLENS FLOWERING TOP
- Active strength
- 1 [hp_Q]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ruta Graveolens
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| RUTA GRAVEOLENS FLOWERING TOP | 1 [hp_Q]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | N94C2U587S |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37662-2269-1 | Ruta Graveolens | 10000 in 1 BOTTLE, GLASS | PELLET | 10000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37662-2269 | RUTA GRAVEOLENS PELLET [HAHNEMANN LABORATORIES, INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20230108_f1a3bd93-80d4-be37-e053-2a95a90a3fd9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37662-2269-1 | 37662226901 | 10000 PELLET in 1 BOTTLE, GLASS (37662-2269-1) | 10000 pellet | 2023-01-06 | 0000-00-00 | No | No | Current |