Nicorette
- Product NDC
- 0135-0226
- 11-digit product format
- 001350226
- Labeler code
- 0135
- Product ID
- 0135-0226_1107242e-6fb9-48c7-a01a-f299b1c90177
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- nicotine polacrilex
- Dosage form
- GUM, CHEWING
- Route
- ORAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- NDA020066
- Marketing category
- NDA
- Marketing start
- 2009-06-29
- Marketing end
- 0000-00-00
- Substance
- NICOTINE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0135-0226-02 | 00135022602 | 1 BLISTER PACK in 1 CARTON (0135-0226-02) > 100 GUM, CHEWING in 1 BLISTER PACK | 1 blister pack | 2009-06-29 | 0000-00-00 | No | No | Current |
| 0135-0226-17 | 00135022617 | 2 CARTON in 1 PACKAGE (0135-0226-17) > 10 BLISTER PACK in 1 CARTON > 10 GUM, CHEWING in 1 BLISTER PACK | 2 carton | 2014-08-01 | 0000-00-00 | No | No | Current |