Betaxolol
- Product NDC
- 60429-754
- 11-digit product format
- 604290754
- Labeler code
- 60429
- Product ID
- 60429-754_b6257ebf-3105-7f4f-e053-2995a90a6cec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Betaxolol
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA078962
- Marketing category
- ANDA
- Marketing start
- 2008-06-27
- Marketing end
- 0000-00-00
- Substance
- BETAXOLOL HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-754-01 | 60429075401 | 100 TABLET, FILM COATED in 1 BOTTLE (60429-754-01) | 2012-06-01 | 0000-00-00 | No | No | Current |