Onopordon comp.
- Product NDC
- 48951-7089
- 11-digit product format
- 489517089
- Labeler code
- 48951
- Product ID
- 48951-7089_6ad919fe-d07a-71b9-e053-2991aa0a46bb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Onopordon comp.
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ONOPORDUM ACANTHIUM FLOWER; PRIMULA VERIS FLOWER; HYOSCYAMUS NIGER LEAF
- Active strength
- 1 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 48951-7089-3 | Onopordon comp. | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-7089 | ONOPORDON COMP. LIQUID [URIEL PHARMACY INC.] | 5 | Legacy NDC, 1 package rows | 20241123_6f61e98d-fd67-42d7-9826-45f35aa21bf5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-7089-3 | 48951708903 | 60 mL in 1 BOTTLE, DROPPER (48951-7089-3) | 60 ml | 2009-09-01 | 0000-00-00 | No | No | Current |