Maxi Nicotine
- Product NDC
- 11822-3319
- 11-digit product format
- 118223319
- Labeler code
- 11822
- Product ID
- 11822-3319_a6c9cb37-474b-4f45-8898-576960f6885f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- nicotine polacrilex
- Dosage form
- LOZENGE
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA210712
- Marketing category
- ANDA
- Marketing start
- 2021-07-09
- Marketing end
- 0000-00-00
- Substance
- NICOTINE
- Active strength
- 4 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 11822-3319 | MAXI NICOTINE (NICOTINE POLACRILEX) LOZENGE [RITE AID CORPORATION] | 4 | Legacy NDC | 20230223_5674ba36-8b62-4e46-81e5-ef2c57bea102.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-3319-0 | 11822331900 | 3 BOTTLE, PLASTIC in 1 BOX (11822-3319-0) > 24 LOZENGE in 1 BOTTLE, PLASTIC | 2020-03-18 | 0000-00-00 | No | No | Current |