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Carbamazepine
Carbamazepine - 51079-870-20 - (Carbamazepine)
Drug Information of Carbamazepine
| Product NDC: | 51079-870 |
| Proprietary Name: | Carbamazepine |
| Non Proprietary Name: | Carbamazepine |
| Active Ingredient(s): | 100 mg/1 & nbsp; Carbamazepine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Carbamazepine
| Product NDC: | 51079-870 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073524 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111028 |
Package Information of Carbamazepine
| Package NDC: | 51079-870-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-870-20) > 1 TABLET, CHEWABLE in 1 BLISTER PACK (51079-870-01) |
NDC Information of Carbamazepine
| NDC Code | 51079-870-20 |
| Proprietary Name | Carbamazepine |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-870-20) > 1 TABLET, CHEWABLE in 1 BLISTER PACK (51079-870-01) |
| Product NDC | 51079-870 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carbamazepine |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20111028 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | CARBAMAZEPINE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
