APO-VARENICLINE
- Product NDC
- 60505-4766
- 11-digit product format
- 605054766
- Labeler code
- 60505
- Product ID
- 60505-4766_3bfed7dd-f8ff-fb1b-f712-7404ac18ca5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VARENICLINE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp
- Marketing category
- UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
- Marketing start
- 2021-07-16
- Marketing end
- 0000-00-00
- Substance
- VARENICLINE TARTRATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Partial Cholinergic Nicotinic Agonist [EPC],Partial Cholinergic Nicotinic Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 60505-4766-5 | 60505476605 | 1 BLISTER PACK in 1 CARTON (60505-4766-5) > 56 TABLET, FILM COATED in 1 BLISTER PACK | 1 blister pack | 2021-07-16 | 0000-00-00 | No | No | Current |
| 60505-4766-6 | 60505476606 | 56 TABLET, FILM COATED in 1 BOTTLE (60505-4766-6) | | 2021-07-16 | 0000-00-00 | No | No | Current |