Tramadol Hydrochloride
- Product NDC
- 67296-1766
- 11-digit product format
- 672961766
- Labeler code
- 67296
- Product ID
- 67296-1766_c0aa5004-a23c-d510-e053-2a95a90a808c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tramadol hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA075986
- Marketing category
- ANDA
- Marketing start
- 2020-01-01
- 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 |
|---|
| 67296-1766-1 | 67296176601 | 10 TABLET, FILM COATED in 1 BOTTLE (67296-1766-1) | 2021-04-01 | 0000-00-00 | No | No | Current |
| 67296-1766-2 | 67296176602 | 20 TABLET, FILM COATED in 1 BOTTLE (67296-1766-2) | 2020-01-01 | 0000-00-00 | No | No | Current |