Petasites Plantago
- Product NDC
- 48951-8020
- 11-digit product format
- 489518020
- Labeler code
- 48951
- Product ID
- 48951-8020_6deb5309-e88d-cec9-e053-2a91aa0a8bfa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Petasites Plantago
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ABIES ALBA LEAFY TWIG; PETASITES HYBRIDUS ROOT; PLANTAGO MAJOR LEAF; FERROSOFERRIC PHOSPHATE; SUS SCROFA LUNG
- Active strength
- 3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- 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 |
|---|
| 48951-8020-2 | 48951802002 | 1350 PELLET in 1 BOTTLE, GLASS (48951-8020-2) | 1350 pellet | 2009-09-01 | 0000-00-00 | No | No | Current |