Tramadol Hydrochloride
- Product NDC
- 68788-8920
- 11-digit product format
- 687888920
- Labeler code
- 68788
- Product ID
- 68788-8920_9aa37e51-1c79-4043-a2f6-d1eaa7f0a5d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- NDA022370
- Marketing category
- NDA
- Marketing start
- 2015-09-18
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 150 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