TRAMADOL HYDROCHLORIDE
- Product NDC
- 68788-9237
- 11-digit product format
- 687889237
- Labeler code
- 68788
- Product ID
- 68788-9237_3a9fcc26-b281-4720-a3b6-fe7ff54f6e0f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAMADOL HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals
- Application
- ANDA201384
- Marketing category
- ANDA
- Marketing start
- 2014-10-06
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROC
- Active strength
- 200 mg/1
- Pharmacologic classes
- Full Opioid Ago
- DEA schedule
- CIV
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record