Tramadol Hydrochloride
- Product NDC
- 70518-0118
- 11-digit product format
- 705180118
- Labeler code
- 70518
- Product ID
- 70518-0118_f19b955d-eff5-8668-e053-2a95a90aea61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076003
- Marketing category
- ANDA
- Marketing start
- 2017-01-12
- 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
- 2024-12-31
- 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 |
|---|
| 70518-0118-1 | 70518011801 | 30 TABLET, COATED in 1 BLISTER PACK (70518-0118-1) | 2017-01-12 | 0000-00-00 | No | No | Current |
| 70518-0118-2 | 70518011802 | 120 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-0118-2) | 2017-02-02 | 0000-00-00 | No | No | Current |
| 70518-0118-4 | 70518011804 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-0118-4) | 2017-09-05 | 0000-00-00 | No | No | Current |
| 70518-0118-5 | 70518011805 | 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-0118-5) | 2020-07-31 | 0000-00-00 | No | No | Current |
| 70518-0118-6 | 70518011806 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-0118-6) | 2020-07-31 | 0000-00-00 | No | No | Current |
| 70518-0118-7 | 70518011807 | 60 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-0118-7) | 2020-08-04 | 0000-00-00 | No | No | Current |
| 70518-0118-8 | 70518011808 | 180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-0118-8) | 2020-08-24 | 0000-00-00 | No | No | Current |
| 70518-0118-9 | 70518011809 | 120 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-0118-9) | 2020-08-27 | 0000-00-00 | No | No | Current |