Methadone Hydrochloride
- Product NDC
- 68094-032
- 11-digit product format
- 680940032
- Labeler code
- 68094
- Product ID
- 68094-032_2e11235a-316f-4740-aa7d-d8c7231cbe27
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methadone Hydrochloride
- Dosage form
- CONCENTRATE
- Route
- ORAL
- Labeler
- Precision Dose, Inc.
- Application
- ANDA040180
- Marketing category
- ANDA
- Marketing start
- 2021-03-15
- Marketing end
- 0000-00-00
- Substance
- METHADONE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68094-032-58 | 68094003258 | 50 BAG in 1 CASE (68094-032-58) > 1 SYRINGE in 1 BAG > .5 mL in 1 SYRINGE (68094-032-01) | 50 bag | 2021-03-15 | 0000-00-00 | No | No | Current |