TRAMADOL HYDROCHLORIDE
- Product NDC
- 68788-8921
- 11-digit product format
- 687888921
- Labeler code
- 68788
- Product ID
- 68788-8921_2d33ccda-4d4f-4f86-b8ac-744135eaba67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAMADOL HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA201384
- Marketing category
- ANDA
- Marketing start
- 2015-09-22
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record