Minocycline Hydrochloride
- Product NDC
- 62135-889
- 11-digit product format
- 621350889
- Labeler code
- 62135
- Product ID
- 62135-889_37c8b548-71eb-bac3-e063-6394a90a7052
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Minocycline Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA065436
- Marketing category
- ANDA
- Marketing start
- 2007-12-26
- Substance
- MINOCYCLINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Prothrombin Activity [PE], 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
- Minocycline Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| MINOCYCLINE HYDROCHLORIDE | 100 mg/1 |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | 0020414E5U |
| Rxcui | 207362, 207364, 403840 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d9c90ddb-dcc8-42af-a94b-505e4488bdc7 | Product name | 1 | 20250623 |
| 9e423e97-a6d9-7bb0-0dcb-343af7c0ff92 | Product name | 2 | 20230322 |
| 472a6924-c7ed-850b-32ce-a510e887fbf9 | Product name | 4 | 20230207 |
| f1239550-2d2e-44c3-aec7-14fd9b4ab55d | Product name | 1 | 20201103 |
| 7a57513a-a145-4b95-9165-1e0ef21d6017 | Product name | 1 | 20200326 |
| 70555e58-6951-4421-9354-f80c6ce0d92c | Product name | 7 | 20200204 |
| 23de08d7-aa4e-ec8b-ce6d-2124a855e4ef | Product name | 5 | 20180605 |
| 76736e48-254d-4a39-993d-206efbdaad1d | Product name | 1 | 20170717 |
| 0c498039-5512-d9d7-e6b6-833de47219ff | Product name | 2 | 20151106 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62135-889-60 | Minocycline Hydrochloride | 60 in 1 BOTTLE | TABLET | 60 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 62135-889-60 | EA - Each | 62135-889 | 17d611b1-bb6a-4545-b082-863c75e04564 | 1 | 2025-07-08 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 207364 | minocycline HCl 100 MG Oral Tablet | PSN | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
| 207362 | minocycline HCl 50 MG Oral Tablet | PSN | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
| 403840 | minocycline HCl 75 MG Oral Tablet | PSN | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
| 207364 | minocycline 100 MG Oral Tablet | SCD | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
| 207362 | minocycline 50 MG Oral Tablet | SCD | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
| 403840 | minocycline 75 MG Oral Tablet | SCD | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
| 207364 | minocycline (as minocycline hydrochloride) 100 MG Oral Tablet | SY | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
| 207362 | minocycline (as minocycline hydrochloride) 50 MG Oral Tablet | SY | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
| 403840 | minocycline (as minocycline hydrochloride) 75 MG Oral Tablet | SY | 43fbe7ff-4b67-474d-bf27-e5710d8d10ac | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 62135-889-60 | 62135088960 | 60 TABLET in 1 BOTTLE (62135-889-60) | 60 tablet | 2025-06-13 | No | No | Historical |