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Carbamazepine
Carbamazepine - 68084-561-21 - (Carbamazepine)
Drug Information of Carbamazepine
| Product NDC: | 68084-561 |
| Proprietary Name: | Carbamazepine |
| Non Proprietary Name: | Carbamazepine |
| Active Ingredient(s): | 200 mg/1 & nbsp; Carbamazepine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Carbamazepine
| Product NDC: | 68084-561 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020234 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20130624 |
Package Information of Carbamazepine
| Package NDC: | 68084-561-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-561-21) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-561-11) |
NDC Information of Carbamazepine
| NDC Code | 68084-561-21 |
| Proprietary Name | Carbamazepine |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-561-21) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-561-11) |
| Product NDC | 68084-561 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carbamazepine |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130624 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | American Health Packaging |
| Substance Name | CARBAMAZEPINE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
