Tramadol Hydrochloride
- Product NDC
- 55154-5656
- 11-digit product format
- 551545656
- Labeler code
- 55154
- Product ID
- 55154-5656_c73fd23f-ceef-4274-9538-127a1811da3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075986
- Marketing category
- ANDA
- Marketing start
- 2011-02-04
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-5656-0 | 55154565600 | 10 BLISTER PACK in 1 BAG (55154-5656-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2011-02-04 | 0000-00-00 | No | No | Current |