Tramadol Hydrochloride
- Product NDC
- 72888-007
- 11-digit product format
- 728880007
- Labeler code
- 72888
- Product ID
- 72888-007_bb58e11c-8a02-1cd1-e053-2a95a90afa56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Advagen Pharma Limited
- Application
- ANDA208708
- Marketing category
- ANDA
- Marketing start
- 2020-09-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72888-007-00 | 72888000700 | 1000 TABLET, COATED in 1 BOTTLE (72888-007-00) | 2020-09-01 | 0000-00-00 | No | No | Current |
| 72888-007-01 | 72888000701 | 100 TABLET, COATED in 1 BOTTLE (72888-007-01) | 2020-09-01 | 0000-00-00 | No | No | Current |
| 72888-007-05 | 72888000705 | 500 TABLET, COATED in 1 BOTTLE (72888-007-05) | 2020-09-01 | 0000-00-00 | No | No | Current |