Pentobarbital Sodium
- Product NDC
- 17478-181
- 11-digit product format
- 174780181
- Labeler code
- 17478
- Product ID
- 17478-181_f0012197-10b0-4fd6-8794-d2ea7ba23378
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pentobarbital Sodium
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA083246
- Marketing category
- ANDA
- Marketing start
- 2019-01-17
- Marketing end
- 0000-00-00
- Substance
- PENTOBARBITAL SODIUM
- Active strength
- 50 mg/mL
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17478-181 | PENTOBARBITAL SODIUM INJECTION [AKORN] | 9 | Legacy NDC | 20240202_0a202fdc-0dc0-4b1a-b858-886914d27c85.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-181-20 | 17478018120 | 1 VIAL, MULTI-DOSE in 1 CARTON (17478-181-20) > 20 mL in 1 VIAL, MULTI-DOSE | 2019-01-17 | 0000-00-00 | No | No | Current |
| 17478-181-50 | 17478018150 | 1 VIAL, MULTI-DOSE in 1 CARTON (17478-181-50) > 50 mL in 1 VIAL, MULTI-DOSE | 2019-01-17 | 0000-00-00 | No | No | Current |