DHEA
- Product NDC
- 43742-0564
- 11-digit product format
- 437420564
- Labeler code
- 43742
- Product ID
- 43742-0564_a77dc7d0-2782-45e4-ae58-1625a00f9c41
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DHEA (Dehydroepiandrosterone)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-01-19
- Substance
- PRASTERONE
- Active strength
- 6 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DHEA
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRASTERONE | 6 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 459AG36T1B |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43742-0564-1 | DHEA | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43742-0564 | DHEA (DHEA (DEHYDROEPIANDROSTERONE)) LIQUID [DESERET BIOLOGICALS, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20240925_d6edd874-495c-4eb5-bf3d-72c2ee41fc88.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0564-1 | 43742056401 | 30 mL in 1 BOTTLE, DROPPER (43742-0564-1) | 30 ml | 2015-01-19 | 0000-00-00 | No | No | Current |