Amantadine Hydrochloride
- Product NDC
- 60687-239
- 11-digit product format
- 606870239
- Labeler code
- 60687
- Product ID
- 60687-239_c77c54cd-cd8e-78da-e053-2a95a90a857a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amantadine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA075060
- Marketing category
- ANDA
- Marketing start
- 2020-08-31
- Marketing end
- 2022-05-31
- Substance
- AMANTADINE HYDROCHLORIDE
- Active strength
- 50 mg/5mL
- Pharmacologic classes
- Influenza A M2 Protein Inhibitor [EPC],M2 Protein Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 60687-239-56 | 60687023956 | 10 TRAY in 1 CASE (60687-239-56) > 10 CUP, UNIT-DOSE in 1 TRAY (60687-239-48) > 10 mL in 1 CUP, UNIT-DOSE (60687-239-42) | 10 tray | 2020-06-15 | 0000-00-00 | No | No | Current |