Roqueforti
- Product NDC
- 49693-1801
- 11-digit product format
- 496931801
- Labeler code
- 49693
- Product ID
- 49693-1801_09feba2f-b6b5-458d-af19-e7ab0c84e93e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Penicillium roqueforti
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- USPharmaCo
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-12-15
- Marketing end
- 0000-00-00
- Substance
- PENICILLIUM ROQUEFORTI
- Active strength
- 4 [hp_X]/10mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 49693-1801-1 | Roqueforti | 10 mL in 1 BOTTLE | LIQUID | 10 | | 1 |
| 49693-1801-1 | Roqueforti | 1 in 1 BOX | LIQUID | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49693-1801 | ROQUEFORTI (PENICILLIUM ROQUEFORTI) LIQUID [USPHARMACO] | 1 | Legacy NDC, 2 package rows | 20091229_cf9f097f-4f20-460a-bc19-ea2a89bdd53c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 49693-1801-1 | 49693180101 | 10 mL in 1 BOTTLE | 10 ml | Historical |