Betaxolol
- Product NDC
- 60429-753
- 11-digit product format
- 604290753
- Labeler code
- 60429
- Product ID
- 60429-753_e5fe2932-8e49-dd4e-e053-2a95a90a0c32
- 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
- 2022-09-30
- Substance
- BETAXOLOL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 60429-753-01 | 60429075301 | 100 TABLET, FILM COATED in 1 BOTTLE (60429-753-01) | 2012-06-01 | 0000-00-00 | No | No | Current |