Methadone Hydrochloride
- Product NDC
- 68462-800
- 11-digit product format
- 684620800
- Labeler code
- 68462
- Product ID
- 68462-800_b34e28d6-4556-4170-b148-d6d37d02930f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methadone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Glenmark Pharmaceuticals, Inc., USA
- Application
- ANDA210484
- Marketing category
- ANDA
- Marketing start
- 2018-08-06
- Marketing end
- 0000-00-00
- Substance
- METHADONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 68462-800-01 | 68462080001 | 100 TABLET in 1 BOTTLE, PLASTIC (68462-800-01) | 100 tablet | 2018-08-06 | 0000-00-00 | No | No | Current |