Tramadol Hydrochloride
- Product NDC
- 60429-588
- 11-digit product format
- 604290588
- Labeler code
- 60429
- Product ID
- 60429-588_d44ede44-4378-1aaa-e053-2995a90a6fa1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA075977
- Marketing category
- ANDA
- Marketing start
- 2002-06-19
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60429-588 | TRAMADOL HYDROCHLORIDE TABLET, FILM COATED [GOLDEN STATE MEDICAL SUPPLY, INC.] | 10 | Legacy NDC | 20240302_41d1db45-4d05-49cb-8de5-9444dcf08a6f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-588-01 | 60429058801 | 100 TABLET, FILM COATED in 1 BOTTLE (60429-588-01) | 2017-06-08 | 0000-00-00 | No | No | Current |
| 60429-588-05 | 60429058805 | 500 TABLET, FILM COATED in 1 BOTTLE (60429-588-05) | 2017-06-08 | 0000-00-00 | No | No | Current |