Oxycodone Hydrochloride
- Product NDC
- 17856-0393
- 11-digit product format
- 178560393
- Labeler code
- 17856
- Product ID
- 17856-0393_f2bbcfcb-b0de-413e-aca1-cc786d10b7c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA203208
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 100 mg/5mL
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 17856-0393-1 | Oxycodone Hydrochloride | 1 mL in 1 SYRINGE, PLASTIC | SOLUTION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0393 | OXYCODONE HYDROCHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORPS] | 2 | Legacy NDC, 1 package rows | 20160629_438290e4-3c2a-4bc4-b08b-37f107fc20d2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-0393-1 | 17856039301 | 1 mL in 1 SYRINGE, PLASTIC | 1 ml | Historical |