Ethosuximide
- Product NDC
- 69387-108
- 11-digit product format
- 693870108
- Labeler code
- 69387
- Product ID
- 69387-108_287c9c89-005d-494c-835c-9b7f19db00e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethosuximide
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Banner Life Sciences LLC.
- Application
- ANDA040430
- Marketing category
- ANDA
- Marketing start
- 2015-06-01
- Marketing end
- 0000-00-00
- Substance
- ETHOSUXIMIDE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69387-108-01 | Ethosuximide | 100 in 1 BOTTLE, PLASTIC | CAPSULE, LIQUID FILLED | 100 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69387-108 | ETHOSUXIMIDE CAPSULE, LIQUID FILLED [BANNER LIFE SCIENCES LLC.] | 1 | Legacy NDC, 1 package rows | 20150611_bfb2be16-9fe1-48bd-b054-25e2b1ed7a20.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69387-108-01 | 69387010801 | 100 in 1 BOTTLE, PLASTIC | Historical |