Tru Relief Nicotine
- Product NDC
- 0113-6000
- 11-digit product format
- 001136000
- Labeler code
- 0113
- Product ID
- 0113-6000_8dee28c9-39c3-48e2-a674-5b7eab92c5e6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Nicotine Polacrilex
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- L. Perrigo Company
- Application
- ANDA203690
- Marketing category
- ANDA
- Marketing start
- 2016-12-01
- Marketing end
- 0000-00-00
- Substance
- NICOTINE
- Active strength
- 2 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 0113-6000 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 0113-6000 | 0113-6000-07 | D | Discontinued by firm | | 2026-07-31 |
Orange Book products#
Application-product, Trade name, Ingredient table| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|
| A203690-001 | NICOTINE POLACRILEX | NICOTINE POLACRILEX | EQ 2MG BASE | TROCHE/LOZENGE / ORAL | | | 2012-10-09 |
| A203690-002 | NICOTINE POLACRILEX | NICOTINE POLACRILEX | EQ 4MG BASE | TROCHE/LOZENGE / ORAL | | | 2012-10-09 |