Tramadol HCl
- Product NDC
- 51655-182
- 11-digit product format
- 516550182
- Labeler code
- 51655
- Product ID
- 51655-182_5bee381f-b14b-e62b-e053-2991aa0a3c2b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tramadol HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Northwind Pharmaceuticals
- Application
- ANDA090404
- Marketing category
- ANDA
- Marketing start
- 2017-10-03
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-182 | TRAMADOL HCL TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS] | 1 | Legacy NDC | 20171020_5bee381f-b14a-e62b-e053-2991aa0a3c2b.zip |