tramadol hydrochloride
- Product NDC
- 50090-3501
- 11-digit product format
- 500903501
- Labeler code
- 50090
- Product ID
- 50090-3501_aa07e2fb-972b-4d53-ad7e-04ca2c7601dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tramadol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075964
- Marketing category
- ANDA
- Marketing start
- 2016-04-06
- 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