Divalproex Sodium
- Product NDC
- 37662-0732
- 11-digit product format
- 376620732
- Labeler code
- 37662
- Product ID
- 37662-0732_e3281609-460b-4982-e053-2995a90a01c5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Hahnemann Laboratories, INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2022-07-06
- Substance
- VALPROATE SODIUM
- Active strength
- 1 [hp_Q]/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Divalproex Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VALPROATE SODIUM | 1 [hp_Q]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5VOM6GYJ0D |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 37662-0732-1 | Divalproex Sodium | 10000 in 1 BOTTLE, GLASS | PELLET | 10000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37662-0732 | DIVALPROEX SODIUM PELLET [HAHNEMANN LABORATORIES, INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20221223_e3281609-460a-4982-e053-2995a90a01c5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 37662-0732-1 | 37662073201 | 10000 PELLET in 1 BOTTLE, GLASS (37662-0732-1) | 10000 pellet | 2022-07-06 | 0000-00-00 | No | No | Current |