Nadolol
- Product NDC
- 70518-4662
- 11-digit product format
- 705184662
- Labeler code
- 70518
- Product ID
- 70518-4662_52197684-ee04-b2c5-e063-6294a90afc94
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nadolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201893
- Marketing category
- ANDA
- Marketing start
- 2026-05-18
- Substance
- NADOLOL
- Active strength
- 40 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nadolol
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NADOLOL | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FEN504330V |
| Rxcui | 198007 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4662-0 | Nadolol | 50 in 1 BOX | TABLET | 50 | | 1 |
| 70518-4662-1 | Nadolol | 1 in 1 POUCH | TABLET | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4662-0 | 70518466200 | 50 POUCH in 1 BOX (70518-4662-0) / 1 TABLET in 1 POUCH (70518-4662-1) | 50 pouch | 2026-05-18 | No | No | Historical |
| 70518-4662-1 | 70518466201 | 1 in 1 POUCH | | | | | Historical |