Ethambutol Hydrochloride
- Product NDC
- 85742-006
- 11-digit product format
- 857420006
- Labeler code
- 85742
- Product ID
- 85742-006_2a57c753-d5e5-4479-845b-614c928d6dc5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ethambutol Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kanchan Healthcare Inc
- Application
- NDA016320
- Marketing category
- NDA
- Marketing start
- 2006-12-15
- Substance
- ETHAMBUTOL HYDROCHLORIDE
- Active strength
- 400 mg/1
- Pharmacologic classes
- Antimycobacterial [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ethambutol Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ETHAMBUTOL HYDROCHLORIDE | 400 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | QE4VW5FO07 |
| Rxcui | 995599, 995607 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85742-006-04 | Ethambutol Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 85742-006-04 | 85742000604 | 100 TABLET, FILM COATED in 1 BOTTLE (85742-006-04) | 2025-08-26 | No | No | Historical |