Ethambutol Hydrochloride
- Product NDC
- 50090-2337
- 11-digit product format
- 500902337
- Labeler code
- 50090
- Product ID
- 50090-2337_1f83e876-4a0b-4aeb-bb0b-bc40f0fd9510
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethambutol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA016320
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2006-12-15
- Marketing end
- 0000-00-00
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-2337-0 | Ethambutol Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 21 |
| 50090-2337-1 | Ethambutol Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 21 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2337 | ETHAMBUTOL HYDROCHLORIDE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 21 | Legacy NDC, 2 package rows | 20210206_55a70cf5-c4b5-450e-9fc5-129077dfdfd6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2337-0 | 50090233700 | 100 TABLET, FILM COATED in 1 BOTTLE (50090-2337-0) | 2016-03-25 | 0000-00-00 | No | No | Current |
| 50090-2337-1 | 50090233701 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-2337-1) | 2020-06-09 | 0000-00-00 | No | No | Current |