Tramadol Hydrochloride
- Product NDC
- 60429-584
- 11-digit product format
- 604290584
- Labeler code
- 60429
- Product ID
- 60429-584_d44e9782-c3fe-988b-e053-2a95a90a1a9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride Extended-Release Tablets
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA200491
- Marketing category
- ANDA
- Marketing start
- 2012-06-27
- 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 |
|---|
| 60429-584-30 | 60429058430 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60429-584-30) | 2016-10-20 | 0000-00-00 | No | No | Current |