TRAMADOL HYDROCHLORIDE
- Product NDC
- 10147-0903
- 11-digit product format
- 101470903
- Labeler code
- 10147
- Product ID
- 10147-0903_d2af68e8-c7e8-4adb-b1d9-6f25f32aba8a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAMADOL HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Patriot Pharmaceuticals, LLC
- Application
- NDA021692
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2006-01-16
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 300 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record