Doxycycline
- Product NDC
- 63629-9410
- 11-digit product format
- 636299410
- Labeler code
- 63629
- Product ID
- 63629-9410_fbac8af2-55e8-4bb5-90f7-4019be864f65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Doxycycline
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA065285
- Marketing category
- ANDA
- Marketing start
- 2005-12-08
- Substance
- DOXYCYCLINE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Tetracycline-class Drug [EPC], Tetracyclines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Doxycycline
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOXYCYCLINE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | N12000U13O |
| Rxcui | 1650142 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-9410-1 | Doxycycline | 20 in 1 BOTTLE | TABLET, FILM COATED | 20 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-9410 | DOXYCYCLINE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 1 | Current NDC, 1 package rows | 20240828_5f22094e-9297-4d1b-a37c-7846481b321e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-9410-1 | 63629941001 | 20 TABLET, FILM COATED in 1 BOTTLE (63629-9410-1) | 2024-08-26 | No | No | Historical |