Mandragora e rad. 3
- Product NDC
- 48951-7014
- 11-digit product format
- 489517014
- Labeler code
- 48951
- Product ID
- 48951-7014_55da7020-9764-4ecc-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Mandragora e rad. 3
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- MANDRAGORA OFFICINARUM ROOT
- Active strength
- 3 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record