METHADONE HYDROCHLORIDE
- Product NDC
- 71335-1106
- 11-digit product format
- 713351106
- Labeler code
- 71335
- Product ID
- 71335-1106_d0a8eaa7-da08-4efe-8544-6a086315f9a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHADONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA006134
- Marketing category
- NDA
- Marketing start
- 1947-08-13
- 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 |
|---|
| 71335-1106-1 | 71335110601 | 90 TABLET in 1 BOTTLE (71335-1106-1) | 90 tablet | 2008-09-12 | 0000-00-00 | No | No | Current |
| 71335-1106-2 | 71335110602 | 30 TABLET in 1 BOTTLE (71335-1106-2) | 30 tablet | 2008-09-12 | 0000-00-00 | No | No | Current |
| 71335-1106-3 | 71335110603 | 120 TABLET in 1 BOTTLE (71335-1106-3) | 120 tablet | 2008-09-12 | 0000-00-00 | No | No | Current |
| 71335-1106-4 | 71335110604 | 112 TABLET in 1 BOTTLE (71335-1106-4) | 112 tablet | 2008-09-12 | 0000-00-00 | No | No | Current |
| 71335-1106-5 | 71335110605 | 60 TABLET in 1 BOTTLE (71335-1106-5) | 60 tablet | 2008-09-12 | 0000-00-00 | No | No | Current |
| 71335-1106-6 | 71335110606 | 180 TABLET in 1 BOTTLE (71335-1106-6) | 180 tablet | 2008-09-12 | 0000-00-00 | No | No | Current |
| 71335-1106-7 | 71335110607 | 28 TABLET in 1 BOTTLE (71335-1106-7) | 28 tablet | 2008-09-12 | 0000-00-00 | No | No | Current |