Tramadol Hydrochloride
- Product NDC
- 57237-238
- 11-digit product format
- 572370238
- Labeler code
- 57237
- Product ID
- 57237-238_7f30ad02-f1b9-4976-85b8-3a4d0a61241b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Citron Pharma LLC
- Application
- ANDA203494
- Marketing category
- ANDA
- Marketing start
- 2014-03-31
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record