Doxycycline
- Product NDC
- 50090-1787
- 11-digit product format
- 500901787
- Labeler code
- 50090
- Product ID
- 50090-1787_83779809-cfbd-4b69-90b4-4b36b2f4d79d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065285
- Marketing category
- ANDA
- Marketing start
- 2005-12-08
- 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
- 2022-12-31
- 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 |
|---|
| 50090-1787-0 | Doxycycline | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-1787 | DOXYCYCLINE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 1 package rows | 20210226_9a267954-678a-4446-9c99-c68763b83b8f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1787-0 | 50090178700 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-1787-0) | 2015-04-20 | 0000-00-00 | No | No | Current |