FENTANYL
- Product NDC
- 55700-772
- 11-digit product format
- 557000772
- Labeler code
- 55700
- Product ID
- 55700-772_447be040-aac5-4a83-b6fb-f28f94f84c40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENTANYL
- Dosage form
- PATCH, EXTENDED RELEASE
- Route
- TRANSDERMAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA077449
- Marketing category
- ANDA
- Marketing start
- 2019-07-19
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-772 | FENTANYL PATCH, EXTENDED RELEASE [QUALITY CARE PRODUCTS, LLC] | 6 | Legacy NDC | 20230714_3bbc19e3-5bf1-495a-b698-3d77f83236e9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-772-05 | 55700077205 | 5 POUCH in 1 CARTON (55700-772-05) > 1 PATCH in 1 POUCH > 72 h in 1 PATCH | 5 pouch | 2019-07-19 | 2026-01-31 | No | No | Current |