Nimodipine
- Product NDC
- 62559-210
- 11-digit product format
- 625590210
- Labeler code
- 62559
- Product ID
- 62559-210_afe779b6-cc7b-42b0-87ba-a932477e170b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nimodipine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA201832
- Marketing category
- ANDA
- Marketing start
- 2015-11-01
- Marketing end
- 2022-09-30
- Substance
- NIMODIPINE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
- 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 |
|---|
| 62559-210-31 | 62559021031 | 30 CAPSULE in 1 CARTON (62559-210-31) | 30 capsule | 2015-11-01 | 0000-00-00 | No | No | Current |
| 62559-210-52 | 62559021052 | 10 CAPSULE in 1 BLISTER PACK (62559-210-52) | 10 capsule | 2015-11-01 | 0000-00-00 | No | No | Current |
| 62559-210-81 | 62559021081 | 100 CAPSULE in 1 CARTON (62559-210-81) | 100 capsule | 2015-11-01 | 0000-00-00 | No | No | Current |