Nimodipine
- Product NDC
- 23155-108
- 11-digit product format
- 231550108
- Labeler code
- 23155
- Product ID
- 23155-108_bedeb898-d41b-4aed-a63f-616c236b6d8d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nimodipine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA076740
- Marketing category
- ANDA
- Marketing start
- 2008-03-21
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 23155-108-00 | 23155010800 | 10 BLISTER PACK in 1 CARTON (23155-108-00) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (23155-108-11) | 10 blister pack | 2008-03-21 | 0000-00-00 | No | No | Current |
| 23155-108-30 | 23155010830 | 3 BLISTER PACK in 1 CARTON (23155-108-30) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (23155-108-11) | 3 blister pack | 2008-03-21 | 0000-00-00 | No | No | Current |