Plantago Primula
- Product NDC
- 48951-8035
- 11-digit product format
- 489518035
- Labeler code
- 48951
- Product ID
- 48951-8035_6dfb41b0-b63a-60db-e053-2991aa0a95a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Plantago Primula
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- PLANTAGO MAJOR LEAF; PRIMULA VERIS FLOWER; HYOSCYAMUS NIGER LEAF
- Active strength
- 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