Phenobarbital Oral Solution
- Product NDC
- 81033-164
- 11-digit product format
- 810330164
- Labeler code
- 81033
- Product ID
- 81033-164_446d8928-62fe-1d8e-e063-6394a90a2fe2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital Oral
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Kesin Pharma Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-11-05
- Substance
- PHENOBARBITAL
- Active strength
- 20 mg/5mL
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Phenobarbital Oral Solution
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PHENOBARBITAL | 20 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | YQE403BP4D |
| Rxcui | 702519 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81033-164-47 | Phenobarbital Oral Solution | 473 mL in 1 BOTTLE, PLASTIC | SOLUTION | 473 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 81033-164-47 | 81033016447 | 473 mL in 1 BOTTLE, PLASTIC (81033-164-47) | 473 ml | 2025-11-05 | No | No | Current |