Tramadol Hydrochloride
- Product NDC
- 70518-2005
- 11-digit product format
- 705182005
- Labeler code
- 70518
- Product ID
- 70518-2005_c599c657-fdc1-8ada-e053-2995a90a7dc5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200491
- Marketing category
- ANDA
- Marketing start
- 2019-04-08
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 200 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2005-0 | 70518200500 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2005-0) | 2019-04-08 | 0000-00-00 | No | No | Current |
| 70518-2005-1 | 70518200501 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2005-1) | 2019-04-30 | 0000-00-00 | No | No | Current |