Tramadol Hydrochloride
- Product NDC
- 66267-843
- 11-digit product format
- 662670843
- Labeler code
- 66267
- Product ID
- 66267-843_9caf7de6-44d3-812e-e053-2a95a90a4077
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA076003
- Marketing category
- ANDA
- Marketing start
- 2010-11-15
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record