Petasites e rad. 1 Special Order
- Product NDC
- 48951-8018
- 11-digit product format
- 489518018
- Labeler code
- 48951
- Product ID
- 48951-8018_6b10c7aa-6028-3d89-e053-2991aa0ae718
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Petasites e rad. 1 Special Order
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- PETASITES HYBRIDUS ROOT
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8018-3 | 48951801803 | 60 mL in 1 BOTTLE, DROPPER (48951-8018-3) | 60 ml | 2009-09-01 | 0000-00-00 | No | No | Current |