Methadone Hydrochloride
- Product NDC
- 63629-1905
- 11-digit product format
- 636291905
- Labeler code
- 63629
- Product ID
- 63629-1905_fe8cad1e-a8ad-437a-87d8-2ebf2b2f0b25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methadone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211228
- Marketing category
- ANDA
- Marketing start
- 2019-01-03
- Marketing end
- 0000-00-00
- Substance
- METHADONE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 63629-1905-1 | 63629190501 | 100 TABLET in 1 BOTTLE (63629-1905-1) | 100 tablet | 2021-02-08 | 0000-00-00 | No | No | Current |