tramadol hydrochloride
- Product NDC
- 66336-915
- 11-digit product format
- 663360915
- Labeler code
- 66336
- Product ID
- 66336-915_54c08b26-940a-468e-9b3d-9bda465caa48
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tramadol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Dispensing Solutions, 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]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66336-915-60 | tramadol hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 66336-915-62 | tramadol hydrochloride | 180 in 1 BOTTLE | TABLET | 180 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66336-915 | TRAMADOL HYDROCHLORIDE TABLET [DISPENSING SOLUTIONS, INC.] | 3 | Legacy NDC, 2 package rows | 20131107_42624fb5-5518-4fae-bf40-5ba69e16240b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 66336-915-60 | 66336091560 | 60 in 1 BOTTLE | Historical |
| 66336-915-62 | 66336091562 | 180 in 1 BOTTLE | Historical |