Oxycodone Hydrochloride
- Product NDC
- 31722-111
- 11-digit product format
- 317220111
- Labeler code
- 31722
- Product ID
- 31722-111_76f2b4ea-6ad1-4bd5-8a1c-c4c04fd91b74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals, Inc.
- Application
- NDA022272
- Marketing category
- NDA
- Marketing start
- 2020-12-23
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-111 | OXYCODONE HYDROCHLORIDE TABLET, EXTENDED RELEASE [CAMBER PHARMACEUTICALS, INC.] | 1 | Legacy NDC | 20210522_e8990bfc-e16c-46b2-a3b6-9c9c883aa72a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 31722-111-01 | 31722011101 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-111-01) | 2020-12-23 | 0000-00-00 | No | No | Current |