Amantadine Hydrochloride
- Product NDC
- 0781-2320
- 11-digit product format
- 007812320
- Labeler code
- 0781
- Product ID
- 0781-2320_4c656ec7-6bab-4946-a0a2-8061f2913d36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amantadine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sandoz Inc.
- Application
- ANDA071293
- Marketing category
- ANDA
- Marketing start
- 1987-02-18
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0781-2320-01 | 00781232001 | 100 CAPSULE in 1 BOTTLE (0781-2320-01) | 100 capsule | 1987-02-18 | 0000-00-00 | No | No | Current |
| 0781-2320-05 | 00781232005 | 500 CAPSULE in 1 BOTTLE (0781-2320-05) | 500 capsule | 1987-02-18 | 0000-00-00 | No | No | Current |