Tramadol Hydrochloride
- Product NDC
- 50090-5094
- 11-digit product format
- 500905094
- Labeler code
- 50090
- Product ID
- 50090-5094_736d9b21-1565-48e2-838c-6a76c349832d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tramadol hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075986
- Marketing category
- ANDA
- Marketing start
- 2002-06-21
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5094-0 | 50090509400 | 33 BLISTER PACK in 1 CARTON (50090-5094-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 33 blister pack | 2020-07-02 | 0000-00-00 | No | No | Current |