tramadol hydrochloride
- Product NDC
- 63629-8190
- 11-digit product format
- 636298190
- Labeler code
- 63629
- Product ID
- 63629-8190_2dc542c1-4a5f-4473-81b3-bd7a84ccd19d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tramadol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075964
- Marketing category
- ANDA
- Marketing start
- 2002-06-22
- 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
- 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 |
|---|
| 63629-8190-1 | 63629819001 | 30 TABLET in 1 BOTTLE (63629-8190-1) | 30 tablet | 2019-07-19 | 0000-00-00 | No | No | Current |
| 63629-8190-2 | 63629819002 | 60 TABLET in 1 BOTTLE (63629-8190-2) | 60 tablet | 2019-08-09 | 0000-00-00 | No | No | Current |