TRIENTINE HYDROCHLORIDE
- Product NDC
- 0527-4068
- 11-digit product format
- 005274068
- Labeler code
- 0527
- Product ID
- 0527-4068_0090a2e0-927a-4284-a88b-b3c4cb7dbbdb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRIENTINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Lannett Company Inc.
- Application
- ANDA211251
- Marketing category
- ANDA
- Marketing start
- 2020-12-22
- Marketing end
- 0000-00-00
- Substance
- TRIENTINE HYDROCHLORIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Metal Chelating Activity [MoA], Metal Chelator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0527-4068-37 | 00527406837 | 1 BOTTLE in 1 CARTON (0527-4068-37) > 100 CAPSULE in 1 BOTTLE | 1 bottle | 2020-12-22 | 0000-00-00 | No | No | Current |