PREGNENOLONE
- Product NDC
- 44911-0201
- 11-digit product format
- 449110201
- Labeler code
- 44911
- Product ID
- 44911-0201_65199e75-c522-415e-99db-721f5f96a937
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pregnenolone
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-09
- Marketing end
- 2023-03-01
- Substance
- PREGNENOLONE
- Active strength
- 30 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0201-1 | 44911020101 | 30 mL in 1 BOTTLE, DROPPER (44911-0201-1) | 30 ml | 2015-07-09 | 2023-03-01 | No | No | Current |