FENTANYL
- Product NDC
- 60505-7013
- 11-digit product format
- 605057013
- Labeler code
- 60505
- Product ID
- 60505-7013_3667df05-f059-309d-c2e7-1b1be5c9388e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENTANYL
- Dosage form
- PATCH, EXTENDED RELEASE
- Route
- TRANSDERMAL
- Labeler
- Apotex Corp.
- Application
- ANDA077449
- Marketing category
- ANDA
- Marketing start
- 2013-04-04
- Marketing end
- 2026-01-31
- Substance
- FENTANYL
- Active strength
- 75 ug/h
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60505-7013 | FENTANYL PATCH, EXTENDED RELEASE [APOTEX CORP.] | 17 | Legacy NDC | 20230714_0ff70df0-2cda-d96c-42a8-3bf180310498.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-7013-2 | 60505701302 | 5 POUCH in 1 CARTON (60505-7013-2) > 1 PATCH in 1 POUCH (60505-7013-0) > 72 h in 1 PATCH | 5 pouch | 2013-04-04 | 0000-00-00 | No | No | Current |