OXYCODONE HYDROCHLORIDE
- Product NDC
- 63629-7399
- 11-digit product format
- 636297399
- Labeler code
- 63629
- Product ID
- 63629-7399_61271f15-11ae-4e4b-a7dc-334f5778fab5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077290
- Marketing category
- ANDA
- Marketing start
- 2012-12-26
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7399-1 | 63629739901 | 60 TABLET in 1 BOTTLE (63629-7399-1) | 60 tablet | 2017-09-20 | 0000-00-00 | No | No | Current |
| 63629-7399-2 | 63629739902 | 90 TABLET in 1 BOTTLE (63629-7399-2) | 90 tablet | 2017-09-20 | 0000-00-00 | No | No | Current |
| 63629-7399-3 | 63629739903 | 28 TABLET in 1 BOTTLE (63629-7399-3) | 28 tablet | 2017-09-20 | 0000-00-00 | No | No | Current |
| 63629-7399-4 | 63629739904 | 30 TABLET in 1 BOTTLE (63629-7399-4) | 30 tablet | 2013-05-31 | 0000-00-00 | No | No | Current |
| 63629-7399-5 | 63629739905 | 8 TABLET in 1 BOTTLE (63629-7399-5) | 8 tablet | 2013-05-31 | 0000-00-00 | No | No | Current |
| 63629-7399-6 | 63629739906 | 6 TABLET in 1 BOTTLE (63629-7399-6) | 6 tablet | 2013-05-31 | 0000-00-00 | No | No | Current |