Carbamazepine
- Product NDC
- 60687-490
- 11-digit product format
- 606870490
- Labeler code
- 60687
- Product ID
- 60687-490_9b3d77ec-f515-0e30-e053-2995a90a6167
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carbamazepine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077272
- Marketing category
- ANDA
- Marketing start
- 2020-01-03
- Marketing end
- 0000-00-00
- Substance
- CARBAMAZEPINE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA],Cytochrome P450 2C19 Inducers [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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-490-01 | 60687049001 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-490-01) > 1 TABLET in 1 BLISTER PACK (60687-490-11) | 100 blister pack | 2020-01-03 | 0000-00-00 | No | No | Current |