Methadone Hydrochloride
- Product NDC
- 60687-214
- 11-digit product format
- 606870214
- Labeler code
- 60687
- Product ID
- 60687-214_e2716c69-73f8-55bd-e053-2a95a90a1e44
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methadone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA203502
- Marketing category
- ANDA
- Marketing start
- 2016-12-20
- Marketing end
- 2023-04-30
- 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
- 0000-00-00
- 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 |
|---|
| 60687-214-01 | 60687021401 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-214-01) > 1 TABLET in 1 BLISTER PACK (60687-214-11) | 100 blister pack | 2016-12-20 | 0000-00-00 | No | No | Current |