Atenolol
- Product NDC
- 13107-170
- 11-digit product format
- 131070170
- Labeler code
- 13107
- Product ID
- 13107-170_b72f170e-bfa6-463c-9345-31f8a37e43e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atenolol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aurolife Pharma LLC
- Application
- ANDA078512
- Marketing category
- ANDA
- Marketing start
- 2011-06-20
- Marketing end
- 0000-00-00
- Substance
- ATENOLOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 13107-170-01 | Atenolol | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 13107-170-99 | Atenolol | 1000 in 1 BOTTLE | TABLET | 1000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 13107-170 | ATENOLOL TABLET [AUROLIFE PHARMA LLC] | 3 | Legacy NDC, 2 package rows | 20110706_308c0bb7-e8cc-4920-8f23-cf8e7c004341.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 13107-170-01 | 13107017001 | 100 in 1 BOTTLE | Historical |
| 13107-170-99 | 13107017099 | 1000 in 1 BOTTLE | Historical |