Tramadol Hydrochloride and Acetaminophen
- Product NDC
- 68788-9267
- 11-digit product format
- 687889267
- Labeler code
- 68788
- Product ID
- 68788-9267_19905fcc-b599-47e6-8815-8db90ba985b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tramadol hydrochloride and acetaminophen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals
- Application
- ANDA077858
- Marketing category
- ANDA
- Marketing start
- 2014-12-23
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROC
- Active strength
- 38 mg/1; 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