Hydrocodone Bitartrate
- Product NDC
- 65224-920
- 11-digit product format
- 652240920
- Labeler code
- 65224
- Product ID
- 65224-920_33bacd82-e63c-4d97-af99-67f7ca782e6d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocodone Bitartrate
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Persion Pharmaceuticals LLC
- Application
- NDA202880
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-10-25
- Marketing end
- 0000-00-00
- Substance
- HYDROCODONE BITARTRATE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Opioid Agonist [EPC],Opioid Agonists [MoA]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65224-920-60 | 65224092060 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65224-920-60) | 2013-10-25 | 0000-00-00 | No | No | Current |