amantadine hydrochloride
- Product NDC
- 69097-925
- 11-digit product format
- 690970925
- Labeler code
- 69097
- Product ID
- 69097-925_7c9106d0-d686-4f9d-a371-d96a3165e535
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- amantadine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cipla USA Inc.
- Application
- ANDA207571
- Marketing category
- ANDA
- Marketing start
- 2017-01-31
- 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
- 2020-12-31
- 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 |
|---|
| 69097-925-12 | 69097092512 | 500 BOTTLE in 1 BOTTLE (69097-925-12) > 100 TABLET in 1 BOTTLE (69097-925-07) | 500 bottle | 2017-01-31 | 0000-00-00 | No | No | Current |