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Somnote
Somnote - 51991-080-51 - (Chloral Hydrate)
Drug Information of Somnote
| Product NDC: | 51991-080 |
| Proprietary Name: | Somnote |
| Non Proprietary Name: | Chloral Hydrate |
| Active Ingredient(s): | 500 mg/1 & nbsp; Chloral Hydrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Somnote
| Product NDC: | 51991-080 |
| Labeler Name: | Breckenridge Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20010101 |
Package Information of Somnote
| Package NDC: | 51991-080-51 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (51991-080-51) > 10 CAPSULE in 1 BLISTER PACK |
NDC Information of Somnote
| NDC Code | 51991-080-51 |
| Proprietary Name | Somnote |
| Package Description | 5 BLISTER PACK in 1 CARTON (51991-080-51) > 10 CAPSULE in 1 BLISTER PACK |
| Product NDC | 51991-080 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chloral Hydrate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20010101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Breckenridge Pharmaceutical, Inc. |
| Substance Name | CHLORAL HYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
