Tramadol Hydrochloride
- Product NDC
- 65862-667
- 11-digit product format
- 658620667
- Labeler code
- 65862
- Product ID
- 65862-667_37e94590-f36e-4269-99f9-898e20dcbfcd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA203494
- Marketing category
- ANDA
- Marketing start
- 2014-03-31
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIV
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65862-667-01 | 65862066701 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-667-01) | 2014-03-31 | 0000-00-00 | No | No | Current |
| 65862-667-05 | 65862066705 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-667-05) | 2014-03-31 | 0000-00-00 | No | No | Current |
| 65862-667-99 | 65862066799 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-667-99) | 2014-03-31 | 0000-00-00 | No | No | Current |