Acebutolol Hydrochloride
- Product NDC
- 51407-666
- 11-digit product format
- 514070666
- Labeler code
- 51407
- Product ID
- 51407-666_462fa6dd-0afc-9a7f-e063-6294a90a5055
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Acebutolol Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA074007
- Marketing category
- ANDA
- Marketing start
- 1995-10-18
- Substance
- ACEBUTOLOL HYDROCHLORIDE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Acebutolol Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACEBUTOLOL HYDROCHLORIDE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | B025Y34C54 |
| Rxcui | 998685, 998689 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-666-01 | Acebutolol Hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-666 | ACEBUTOLOL HYDROCHLORIDE CAPSULE [GOLDEN STATE MEDICAL SUPPLY, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20230325_f037a079-fde6-3588-e053-2995a90a6621.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-666-01 | 51407066601 | 100 CAPSULE in 1 BOTTLE (51407-666-01) | 100 capsule | 2022-08-01 | 0000-00-00 | No | No | Current |