Nadolol
- Product NDC
- 60687-898
- 11-digit product format
- 606870898
- Labeler code
- 60687
- Product ID
- 60687-898_40d197a4-871c-104b-e063-6394a90a69fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA210955
- Marketing category
- ANDA
- Marketing start
- 2025-10-08
- Substance
- NADOLOL
- Active strength
- 40 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
- Nadolol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NADOLOL | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FEN504330V |
| Rxcui | 198006, 198007 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-898-11 | Nadolol | 1 in 1 BLISTER PACK | TABLET | 1 | | 2 |
| 60687-898-21 | Nadolol | 30 in 1 CARTON | TABLET | 30 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60687-898-11 | 60687089811 | 1 in 1 BLISTER PACK | | | | | Historical |
| 60687-898-21 | 60687089821 | 30 BLISTER PACK in 1 CARTON (60687-898-21) / 1 TABLET in 1 BLISTER PACK (60687-898-11) | 30 blister pack | 2025-10-08 | No | No | Current |