Salsolinol
- Product NDC
- 43742-0303
- 11-digit product format
- 437420303
- Labeler code
- 43742
- Product ID
- 43742-0303_2f38346d-5b60-4f35-a6a2-f646a9f12b89
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Salsolinol
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-01-09
- Marketing end
- 2019-12-29
- Substance
- SALSOLINOL
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record