TRAMADOL HYDROCHLORIDE
- Product NDC
- 60760-319
- 11-digit product format
- 607600319
- Labeler code
- 60760
- Product ID
- 60760-319_88c6fbad-e52d-3e66-e053-2a95a90adcbc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRAMADOL HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA090404
- Marketing category
- ANDA
- Marketing start
- 2011-01-31
- 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
- 2020-12-31
- 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 |
|---|
| 60760-319-09 | 60760031909 | 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-319-09) | 2018-01-22 | 0000-00-00 | No | No | Current |
| 60760-319-20 | 60760031920 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-319-20) | 2017-12-04 | 0000-00-00 | No | No | Current |
| 60760-319-30 | 60760031930 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-319-30) | 2017-12-04 | 0000-00-00 | No | No | Current |
| 60760-319-50 | 60760031950 | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-319-50) | 2018-06-28 | 0000-00-00 | No | No | Current |
| 60760-319-60 | 60760031960 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-319-60) | 2017-12-04 | 0000-00-00 | No | No | Current |
| 60760-319-90 | 60760031990 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-319-90) | 2018-04-24 | 0000-00-00 | No | No | Current |