Tramadol Hydrochloride
- Product NDC
- 70518-3598
- 11-digit product format
- 705183598
- Labeler code
- 70518
- Product ID
- 70518-3598_f0e89a00-f74f-270e-e053-2a95a90a24e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075977
- Marketing category
- ANDA
- Marketing start
- 2022-12-23
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3598-0 | 70518359800 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3598-0) | 2022-12-23 | 0000-00-00 | No | No | Current |
| 70518-3598-1 | 70518359801 | 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3598-1) | 2022-12-28 | 0000-00-00 | No | No | Current |