OXYCODONE HYDROCHLORIDE
- Product NDC
- 61919-821
- 11-digit product format
- 619190821
- Labeler code
- 61919
- Product ID
- 61919-821_8d2c450a-a72f-39ed-e053-2995a90abd5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA203638
- Marketing category
- ANDA
- Marketing start
- 2019-07-08
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- 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 |
|---|
| 61919-821-30 | OXYCODONE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-821 | OXYCODONE HYDROCHLORIDE TABLET [DIRECT_RX] | 1 | Legacy NDC, 1 package rows | 20190607_8a9529a3-8922-6b50-e053-2995a90a4b08.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-821-30 | 61919082130 | 30 in 1 BOTTLE | Historical |