Ruta graveolens
- Product NDC
- 71919-595
- 11-digit product format
- 719190595
- Labeler code
- 71919
- Product ID
- 71919-595_3c3e9995-41a8-49d6-b1c6-b608084bb437
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- RUTA GRAVEOLENS FLOWERING TOP
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Washington Homeopathic Products
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-12-31
- Marketing end
- 0000-00-00
- Substance
- RUTA GRAVEOLENS FLOWERING TOP
- Active strength
- 30 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71919-595-07 | Ruta graveolens | 15 mL in 1 VIAL, GLASS | LIQUID | 15 | | 1 |
| 71919-595-08 | Ruta graveolens | 30 mL in 1 VIAL, GLASS | LIQUID | 30 | | 1 |
| 71919-595-09 | Ruta graveolens | 50 mL in 1 BOTTLE, GLASS | LIQUID | 50 | | 1 |
| 71919-595-10 | Ruta graveolens | 100 mL in 1 BOTTLE, GLASS | LIQUID | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71919-595 | RUTA GRAVEOLENS (RUTA GRAVEOLENS FLOWERING TOP) LIQUID [WASHINGTON HOMEOPATHIC PRODUCTS] | 1 | Legacy NDC, 4 package rows | 20180516_72420c17-858b-4d21-b60b-b9e0c39719e2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71919-595-07 | 71919059507 | 15 mL in 1 VIAL, GLASS | 15 ml | Historical |
| 71919-595-08 | 71919059508 | 30 mL in 1 VIAL, GLASS | 30 ml | Historical |
| 71919-595-09 | 71919059509 | 50 mL in 1 BOTTLE, GLASS | 50 ml | Historical |
| 71919-595-10 | 71919059510 | 100 mL in 1 BOTTLE, GLASS | 100 ml | Historical |