Phenobarbital
- Product NDC
- 70166-537
- 11-digit product format
- 701660537
- Labeler code
- 70166
- Product ID
- 70166-537_8a33bf54-9556-4e92-e053-2a95a90ab053
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Lohxa, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-05-31
- Marketing end
- 0000-00-00
- Substance
- PHENOBARBITAL
- Active strength
- 20 mg/5mL
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70166-537-05 | Phenobarbital | 30 in 1 BOX | LIQUID | 30 | | 1 |
| 70166-537-05 | Phenobarbital | 5 mL in 1 CUP, UNIT-DOSE | LIQUID | 5 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70166-537 | PHENOBARBITAL LIQUID [LOHXA, LLC] | 1 | Legacy NDC, 2 package rows | 20190601_1fc1d779-7dd5-4f98-be67-a5ab710faf69.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70166-537-05 | 70166053705 | 30 CUP, UNIT-DOSE in 1 BOX (70166-537-05) > 5 mL in 1 CUP, UNIT-DOSE | 2019-05-31 | 0000-00-00 | No | No | Current |