Oxycodone Hydrochloride
- Product NDC
- 62559-167
- 11-digit product format
- 625590167
- Labeler code
- 62559
- Product ID
- 62559-167_d6bf3c12-70dd-4089-b3ed-0d22371efbd2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA205177
- Marketing category
- ANDA
- Marketing start
- 2016-06-10
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Oxycodone Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OXYCODONE HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C1ENJ2TE6C |
| Rxcui | 1049696 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62559-167-01 | Oxycodone Hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62559-167 | OXYCODONE HYDROCHLORIDE CAPSULE [ANI PHARMACEUTICALS, INC.] | 9 | Current NDC, Legacy NDC, 1 package rows | 20240509_5df92fed-6194-4905-9ef2-9eed0d2e8086.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 |
|---|
| 62559-167-01 | 62559016701 | 100 CAPSULE in 1 BOTTLE (62559-167-01) | 100 capsule | 2016-06-10 | 0000-00-00 | No | No | Current |