NDC 29300-468 – Clonidine hydrochloride
Clonidine Hydrochloride .1 mg/1 · Tablet · Oral
Product NDC29300-468
Product details
- Brand name
- Clonidine hydrochloride
- Generic name
- Clonidine hydrochloride
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078895
- Marketed since
- December 24, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Central alpha-2 Adrenergic Agonist
Active ingredients
- Clonidine Hydrochloride .1 mg/1
Uses, dosage, side effects and warnings for Clonidine Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 29300-468-01 | 100 TABLET in 1 BOTTLE, PLASTIC (29300-468-01) | Dec 24, 2020 |
| 29300-468-05 | 500 TABLET in 1 BOTTLE, PLASTIC (29300-468-05) | Dec 24, 2020 |
| 29300-468-10 | 1000 TABLET in 1 BOTTLE, PLASTIC (29300-468-10) | Dec 24, 2020 |
| 29300-468-50 | 5000 TABLET in 1 BOTTLE, PLASTIC (29300-468-50) | Dec 24, 2020 |
Recalls mentioning this NDC
- D-1541-2022 Sep 28, 2022 · Class III
Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a 100-count bottle of 0.3 mg strength Clonidine Hydrochloride Tablets, - D-1291-2020 Jun 17, 2020 · Class III
Failed Impurities/Degradation Specifications: potential migration of benzophenone at very low level into the product from container. - D-0829-2020 Feb 12, 2020 · Class III
Failed Impurities/Degredation Specifications: This recall is initiated as a precautionary measure due to potential migration of Benzophenone at very low level into product from container label.
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