Doxycycline
- Product NDC
- 61919-474
- 11-digit product format
- 619190474
- Labeler code
- 61919
- Product ID
- 61919-474_9c93c4a2-a5a1-5060-e053-2a95a90afd72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA091605
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- DOXYCYCLINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC],Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 61919-474-20 | Doxycycline | 20 in 1 BOTTLE | TABLET | 20 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-474 | DOXYCYCLINE TABLET [DIRECT RX] | 3 | Legacy NDC, 1 package rows | 20200121_3f51c8ca-bf19-48b8-ac69-3830bff45087.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 |
|---|
| 61919-474-20 | 61919047420 | 20 TABLET in 1 BOTTLE (61919-474-20) | 20 tablet | 2015-01-01 | 0000-00-00 | No | No | Current |