tramadol hydrochloride
- Product NDC
- 68071-5142
- 11-digit product format
- 680715142
- Labeler code
- 68071
- Product ID
- 68071-5142_e1f6a6b1-120d-0ea5-e053-2995a90a6d4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tramadol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA075964
- Marketing category
- ANDA
- Marketing start
- 2002-06-22
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-5142-2 | tramadol hydrochloride | 12 in 1 BOTTLE | TABLET | 12 | | 4 |
| 68071-5142-6 | tramadol hydrochloride | 6 in 1 BOTTLE | TABLET | 6 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-5142 | TRAMADOL HYDROCHLORIDE TABLET [NUCARE PHARMACEUTICALS,INC.] | 4 | Legacy NDC, 2 package rows | 20240621_9ba9c68c-ff27-eb24-e053-2a95a90ae21c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-5142-2 | 68071514202 | 12 TABLET in 1 BOTTLE (68071-5142-2) | 12 tablet | 2020-01-08 | 0000-00-00 | No | No | Current |
| 68071-5142-6 | 68071514206 | 6 TABLET in 1 BOTTLE (68071-5142-6) | 6 tablet | 2020-01-08 | 0000-00-00 | No | No | Current |