Tramadol Hydrochloride
- Product NDC
- 67046-730
- 11-digit product format
- 670460730
- Labeler code
- 67046
- Product ID
- 67046-730_a1527d3b-85a5-4588-8ce3-533ecb48ab7f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA076003
- Marketing category
- ANDA
- Marketing start
- 2010-02-26
- Marketing end
- 0000-00-00
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |