amantadine hydrochloride
- Product NDC
- 68788-6975
- 11-digit product format
- 687886975
- Labeler code
- 68788
- Product ID
- 68788-6975_711aab99-852a-4933-9c7e-c25276011ed4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amantadine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA208278
- Marketing category
- ANDA
- Marketing start
- 2016-08-04
- Marketing end
- 0000-00-00
- Substance
- AMANTADINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [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 |
|---|
| 68788-6975-1 | 68788697501 | 30 CAPSULE in 1 BOTTLE (68788-6975-1) | 30 capsule | 2017-06-06 | 0000-00-00 | No | No | Current |
| 68788-6975-2 | 68788697502 | 20 CAPSULE in 1 BOTTLE (68788-6975-2) | 20 capsule | 2017-06-06 | 0000-00-00 | No | No | Current |
| 68788-6975-3 | 68788697503 | 30 CAPSULE in 1 BOTTLE (68788-6975-3) | 30 capsule | 2017-06-06 | 0000-00-00 | No | No | Current |
| 68788-6975-4 | 68788697504 | 14 CAPSULE in 1 BOTTLE (68788-6975-4) | 14 capsule | 2017-06-06 | 0000-00-00 | No | No | Current |