Tramadol Hydrochloride
- Product NDC
- 10370-222
- 11-digit product format
- 103700222
- Labeler code
- 10370
- Product ID
- 10370-222_db277e3d-eeed-4af9-b0a0-c4d561a02737
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol Hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA200491
- Marketing category
- ANDA
- Marketing start
- 2012-06-27
- Marketing end
- 2022-01-31
- Substance
- TRAMADOL HYDROCHLORIDE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 10370-222-11 | 10370022211 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-222-11) | 2012-06-27 | 0000-00-00 | No | No | Current |