Octopamine
- Product NDC
- 43742-0975
- 11-digit product format
- 437420975
- Labeler code
- 43742
- Product ID
- 43742-0975_fa7f6064-adf4-40be-a145-ef0aa0c0cb81
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octopamine (Hydrochloride)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2017-02-16
- Marketing end
- 2022-03-16
- Substance
- OCTOPAMINE HYDROCHLORIDE
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 43742-0975-1 | 43742097501 | 30 mL in 1 BOTTLE, DROPPER (43742-0975-1) | 30 ml | 2017-02-16 | 2022-03-16 | No | No | Current |