Methadone Hydrochloride
- Product NDC
- 55700-882
- 11-digit product format
- 557000882
- Labeler code
- 55700
- Product ID
- 55700-882_21320d86-ab63-439c-bcef-a374bcf54bb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methadone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA090635
- Marketing category
- ANDA
- Marketing start
- 2020-10-02
- 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 |
|---|
| 55700-882-01 | 55700088201 | 120 TABLET in 1 BOTTLE (55700-882-01) | 120 tablet | 2020-10-02 | 0000-00-00 | No | No | Current |
| 55700-882-30 | 55700088230 | 30 TABLET in 1 BOTTLE (55700-882-30) | 30 tablet | 2020-10-02 | 0000-00-00 | No | No | Current |
| 55700-882-60 | 55700088260 | 60 TABLET in 1 BOTTLE (55700-882-60) | 60 tablet | 2020-10-02 | 0000-00-00 | No | No | Current |
| 55700-882-90 | 55700088290 | 90 TABLET in 1 BOTTLE (55700-882-90) | 90 tablet | 2020-10-02 | 0000-00-00 | No | No | Current |