Tramadol Hydrochloride
- Product NDC
- 60760-622
- 11-digit product format
- 607600622
- Labeler code
- 60760
- Product ID
- 60760-622_7b2fb1b0-5970-7402-e053-2991aa0a2cb2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA076003
- Marketing category
- ANDA
- Marketing start
- 2010-11-15
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 9N7R477WCK | TRAMADOL HYDROCHLORIDE | 36282-47-0 | TRAMADOL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-622-09 | 60760062209 | 9 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-622-09) | 2017-12-15 | 0000-00-00 | No | No | Current |
| 60760-622-90 | 60760062290 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-622-90) | 2017-12-15 | 0000-00-00 | No | No | Current |